Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 196394 |
| ensemblid | ENSG00000151743.11 |
| hgncid | 27281 |
| symbol | AMN1 |
| name | antagonist of mitotic exit network 1 homolog |
| refseq_nuc | NM_001113402.2 |
| refseq_prot | NP_001106873.1 |
| ensembl_nuc | ENST00000281471.11 |
| ensembl_prot | ENSP00000281471.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 31671142 |
| end | 31729021 |
| strand | - |
| ver | v1.2 |
| region | chr12:31671142-31729021 |
| region5000 | chr12:31666142-31734021 |
| regionname0 | AMN1_chr12_31671142_31729021 |
| regionname5000 | AMN1_chr12_31666142_31734021 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 258 | 431 | 98 | 75 | 202 | 16 | 38 | 154 | AMN1_chr12_31666142_31734021 | AMN1 | MPRPR others(253): Show |
chr12 | 31666142 | 31734021 |
| a0002 | 0/0 | 258 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | MPRPR others(253): Show |
chr12 | 31666142 | 31734021 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 774 | 426 | 93 | 75 | 202 | 16 | 38 | AMN1_chr12_31666142_31734021 | AMN1 | ATGCC others(769): Show |
chr12 | 31666142 | 31734021 | ||
| a0001c0002 | 0/0 | 774 | 4 | 4 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | ATGCC others(769): Show |
chr12 | 31666142 | 31734021 | ||
| a0001c0004 | 0/0 | 774 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | ATGCC others(769): Show |
chr12 | 31666142 | 31734021 | ||
| a0002c0003 | 0/0 | 774 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | ATGCC others(769): Show |
chr12 | 31666142 | 31734021 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1952 | 296 | 50 | 52 | 157 | 8 | 28 | AMN1_chr12_31666142_31734021 | AMN1 | AGACG others(1947): Show |
chr12 | 31666142 | 31734021 |
| a0001c0001t0002 | 0/1 | 1952 | 83 | 23 | 15 | 29 | 7 | 8 | AMN1_chr12_31666142_31734021 | AMN1 | AGACG others(1947): Show |
chr12 | 31666142 | 31734021 |
| a0001c0001t0003 | 0/0 | 1952 | 27 | 8 | 4 | 13 | 1 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | AGACG others(1947): Show |
chr12 | 31666142 | 31734021 |
| a0001c0001t0004 | 0/0 | 1952 | 6 | 6 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | AGACG others(1947): Show |
chr12 | 31666142 | 31734021 |
| a0001c0001t0005 | 0/0 | 1954 | 5 | 5 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | AGACG others(1949): Show |
chr12 | 31666142 | 31734021 |
| a0001c0001t0006 | 0/0 | 1952 | 4 | 0 | 4 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | AGACG others(1947): Show |
chr12 | 31666142 | 31734021 |
| a0001c0001t0008 | 0/0 | 1963 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | AGACG others(1958): Show |
chr12 | 31666142 | 31734021 |
| a0001c0001t0009 | 0/0 | 1952 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | AGACG others(1947): Show |
chr12 | 31666142 | 31734021 |
| a0001c0001t0010 | 0/0 | 1952 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | AGACG others(1947): Show |
chr12 | 31666142 | 31734021 |
| a0001c0001t0011 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | AGACG others(1947): Show |
chr12 | 31666142 | 31734021 |
| a0001c0001t0012 | 0/0 | 1952 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | AGACG others(1947): Show |
chr12 | 31666142 | 31734021 |
| a0001c0002t0001 | 0/0 | 1952 | 2 | 2 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | AGACG others(1947): Show |
chr12 | 31666142 | 31734021 |
| a0001c0002t0007 | 0/0 | 1952 | 2 | 2 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | AGACG others(1947): Show |
chr12 | 31666142 | 31734021 |
| a0001c0004t0002 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | AGACG others(1947): Show |
chr12 | 31666142 | 31734021 |
| a0002c0003t0001 | 0/0 | 1952 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | AGACG others(1947): Show |
chr12 | 31666142 | 31734021 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0008 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0010 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0028 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0169 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0002g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0003g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0005g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0005g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0005g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0005g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0005g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0006g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0006g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0008g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0009g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0010g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0011g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0001t0012g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0002t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0002t0007g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0001c0004t0002g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| a0002c0003t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0369 | EUR | GBR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0168 | EUR | GBR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0162 | EUR | FIN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0328 | EUR | FIN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | FIN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | CHS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | CHS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0377 | EAS | CHS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | CHS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | CHS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0366 | EAS | CHS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | CHS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | CHS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | CHS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0099 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0370 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0359 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0119 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0176 | EUR | IBS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0199 | EUR | IBS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0164 | EUR | IBS | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0055 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01934 | hp2 | a0002 | c0003 | t0001 | g0282 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0101 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01975 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02004 | hp2 | a0001 | c0001 | t0006 | g0100 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02071 | hp1 | a0001 | c0001 | t0012 | g0096 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0084 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02148 | hp1 | a0001 | c0001 | t0006 | g0015 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | CDX | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | CDX | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | CDX | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | CDX | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0379 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | KHV | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02602 | hp1 | a0001 | c0001 | t0009 | g0360 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0321 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0237 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0372 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0273 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | ESN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0381 | AFR | ESN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0085 | AFR | MSL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0371 | AFR | MSL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03130 | hp1 | a0001 | c0001 | t0011 | g0382 | AFR | ESN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | ESN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03195 | hp1 | a0001 | c0004 | t0002 | g0383 | AFR | ESN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0373 | AFR | ESN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | MSL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | MSL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0103 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | ESN | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | MSL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03579 | hp2 | a0001 | c0002 | t0007 | g0275 | AFR | MSL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0356 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | STU | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0333 | SAS | STU | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0362 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0357 | SAS | BEB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | BEB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | STU | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | STU | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | BEB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0330 | SAS | STU | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | STU | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | STU | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0367 | SAS | STU | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0086 | AFR | YRI | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | YRI | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | CHB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | CHB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18959 | hp2 | a0001 | c0001 | t0010 | g0213 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0378 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18978 | hp2 | a0001 | c0001 | t0008 | g0353 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | LWK | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | LWK | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | LWK | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0376 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | YRI | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0380 | AFR | YRI | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ASW | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0183 | EUR | TSI | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0105 | EUR | TSI | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0179 | EUR | TSI | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | CLM | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG02559 | hp2 | a0001 | c0002 | t0007 | g0274 | AFR | ACB | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0375 | AFR | MSL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | MSL | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | USA | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | USA | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | USA | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0374 | AFR | USA | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | LWK | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0169 | REF | REF | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0028 | REF | REF | AMN1_chr12_31666142_31734021 | AMN1 | chr12 | 31666142 | 31734021 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:31689042 | C | T | 1 | a0002 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.668G>A | p.Arg223His | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/7 | 681/1952 | 668/777 | 223/258 | chr12 | 31689042 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:31672360 | A | G | 1 | a0001c0002 | 4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
synonymous_variant | LOW | c.721T>C | p.Leu241Leu | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 7/7 | 734/1952 | 721/777 | 241/258 | chr12 | 31672360 | |||
| chr12:31729000 | G | C | 1 | a0001c0004 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.9C>G | p.Arg3Arg | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/7 | 22/1952 | 9/777 | 3/258 | chr12 | 31729000 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:31671176 | T | C | 1 | a0001c0001t0011 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1128A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 7/7 | 1128 | chr12 | 31671176 | ||||||
| chr12:31671242 | C | A | 1 | a0001c0002t0007 | 2 | HG02559.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1062G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 7/7 | 1062 | chr12 | 31671242 | ||||||
| chr12:31671431 | G | C | 1 | a0001c0001t0009 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*873C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 7/7 | 873 | chr12 | 31671431 | ||||||
| chr12:31671446 | C | CTA | 1 | a0001c0001t0005 | 5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*856_*857dupTA | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 7/7 | 857 | chr12 | 31671446 | ||||||
| chr12:31671613 | A | C | 1 | a0001c0001t0005 | 5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*691T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 7/7 | 691 | chr12 | 31671613 | ||||||
| chr12:31671660 | T | A | 1 | a0001c0001t0012 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*644A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 7/7 | 644 | chr12 | 31671660 | ||||||
| chr12:31671675 | A | AAGAGTAG others(4): Show |
1 | a0001c0001t0008 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*618_*628dupATGGCT others(5): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 7/7 | 628 | chr12 | 31671675 | ||||||
| chr12:31671766 | C | T | 1 | a0001c0001t0004 | 6 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*538G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 7/7 | 538 | chr12 | 31671766 | ||||||
| chr12:31671977 | G | A | 1 | a0001c0001t0010 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*327C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 7/7 | 327 | chr12 | 31671977 | ||||||
| chr12:31672037 | T | C | 4 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(1): Show |
88 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*267A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 7/7 | 267 | chr12 | 31672037 | ||||||
| chr12:31672089 | C | T | 1 | a0001c0001t0006 | 4 | HG01943.hp2 HG01975.hp2 HG02004.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*215G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 7/7 | 215 | chr12 | 31672089 | ||||||
| chr12:31672186 | G | C | 2 | a0001c0001t0003 a0001c0001t0012 |
28 | HG00733.hp1 HG00735.hp2 HG01175.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*118C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 7/7 | 118 | chr12 | 31672186 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:31672391 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0147 a0001c0001t0001g0148 |
4 | HG02055.hp2 HG02965.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-14G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31672391 | |||||||
| chr12:31672401 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.704-24T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31672401 | |||||||
| chr12:31672592 | G | T | 1 | a0001c0001t0001g0073 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.704-215C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31672592 | |||||||
| chr12:31672811 | AGGTAC | A | 65 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(62): Show |
70 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.704-439_704-435del others(5): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31672811 | |||||||
| chr12:31672858 | A | G | 369 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(366): Show |
417 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(414): Show |
intron_variant | MODIFIER | c.704-481T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31672858 | |||||||
| chr12:31673121 | T | G | 6 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0001c0001t0004g0055 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-744A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31673121 | |||||||
| chr12:31673168 | C | T | 1 | a0001c0001t0004g0237 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.704-791G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31673168 | |||||||
| chr12:31673209 | G | C | 1 | a0001c0001t0009g0360 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.704-832C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31673209 | |||||||
| chr12:31673217 | T | G | 1 | a0001c0001t0001g0283 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.704-840A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31673217 | |||||||
| chr12:31673257 | G | GA | 62 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(59): Show |
66 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.704-881dupT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31673257 | |||||||
| chr12:31673258 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.704-881T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31673258 | |||||||
| chr12:31673508 | A | G | 45 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0036 others(42): Show |
48 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.704-1131T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31673508 | |||||||
| chr12:31673510 | A | G | 284 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(281): Show |
323 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.704-1133T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31673510 | |||||||
| chr12:31673535 | A | G | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-1158T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31673535 | |||||||
| chr12:31673569 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0256 a0001c0001t0001g0258 |
5 | NA18942.hp2 NA18983.hp2 NA19068.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-1192A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31673569 | |||||||
| chr12:31673588 | T | C | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-1211A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31673588 | |||||||
| chr12:31673618 | T | G | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-1241A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31673618 | |||||||
| chr12:31673763 | A | G | 1 | a0001c0001t0001g0358 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.704-1386T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31673763 | |||||||
| chr12:31673844 | T | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(56): Show |
63 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.704-1467A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31673844 | |||||||
| chr12:31673857 | T | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0024 others(47): Show |
64 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.704-1480A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31673857 | |||||||
| chr12:31673857 | T | G | 1 | a0001c0001t0001g0032 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.704-1480A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31673857 | |||||||
| chr12:31673987 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.704-1610G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31673987 | |||||||
| chr12:31674013 | C | CT | 6 | a0001c0001t0002g0198 a0001c0001t0005g0371 a0001c0001t0005g0372 others(3): Show |
6 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-1637dupA | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31674013 | |||||||
| chr12:31674032 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.704-1655G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31674032 | |||||||
| chr12:31674124 | T | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0147 a0001c0001t0001g0148 |
4 | HG02055.hp2 HG02965.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-1747A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31674124 | |||||||
| chr12:31674340 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0327 a0001c0001t0001g0328 |
4 | HG00323.hp1 NA18952.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-1963C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31674340 | |||||||
| chr12:31674395 | G | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0024 others(22): Show |
37 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.704-2018C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31674395 | |||||||
| chr12:31674452 | G | A | 2 | a0001c0001t0001g0340 a0001c0001t0001g0349 |
2 | NA19003.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.704-2075C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31674452 | |||||||
| chr12:31674784 | T | TGAG | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-2410_704-2408d others(5): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31674784 | |||||||
| chr12:31674838 | A | T | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-2461T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31674838 | |||||||
| chr12:31674937 | G | A | 1 | a0001c0001t0004g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.704-2560C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31674937 | |||||||
| chr12:31675021 | C | CA | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(123): Show |
152 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.704-2645dupT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31675021 | |||||||
| chr12:31675021 | CA | C | 71 | a0001c0001t0001g0073 a0001c0001t0001g0111 a0001c0001t0001g0317 others(68): Show |
78 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.704-2645delT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31675021 | |||||||
| chr12:31675044 | C | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0071 |
2 | HG01361.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.704-2667G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31675044 | |||||||
| chr12:31675060 | ATGCTCAT others(2058): Show |
A | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-4748_704-2684d others(2): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31675060 | |||||||
| chr12:31675072 | C | T | 1 | a0001c0001t0001g0370 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.704-2695G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31675072 | |||||||
| chr12:31675128 | C | T | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-2751G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31675128 | |||||||
| chr12:31675188 | C | T | 45 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0036 others(42): Show |
48 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.704-2811G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31675188 | |||||||
| chr12:31675193 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.704-2816C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31675193 | |||||||
| chr12:31675363 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.704-2986C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31675363 | |||||||
| chr12:31675496 | C | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.704-3119G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31675496 | |||||||
| chr12:31675515 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.704-3138C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31675515 | |||||||
| chr12:31675636 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0144 a0001c0001t0001g0145 others(2): Show |
6 | HG02055.hp2 HG02647.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-3259T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31675636 | |||||||
| chr12:31675646 | A | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-3269T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31675646 | |||||||
| chr12:31675648 | C | T | 6 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0330 others(3): Show |
6 | HG03239.hp1 HG03654.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-3271G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31675648 | |||||||
| chr12:31675696 | A | G | 1 | a0001c0001t0001g0309 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.704-3319T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31675696 | |||||||
| chr12:31675944 | T | C | 1 | a0001c0001t0001g0344 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.704-3567A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31675944 | |||||||
| chr12:31676008 | C | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0348 |
2 | NA18939.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.704-3631G>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31676008 | |||||||
| chr12:31676056 | A | G | 9 | a0001c0001t0002g0016 a0001c0001t0002g0116 a0001c0001t0002g0117 others(6): Show |
10 | HG02451.hp2 HG02723.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.704-3679T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31676056 | |||||||
| chr12:31676334 | G | A | 64 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(61): Show |
69 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.704-3957C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31676334 | |||||||
| chr12:31676390 | G | A | 19 | a0001c0001t0001g0030 a0001c0001t0001g0326 a0001c0001t0001g0327 others(16): Show |
19 | HG00323.hp1 HG00423.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.704-4013C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31676390 | |||||||
| chr12:31676439 | G | A | 1 | a0001c0001t0003g0098 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.704-4062C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31676439 | |||||||
| chr12:31676475 | G | GC | 13 | a0001c0001t0001g0024 a0001c0001t0001g0073 a0001c0001t0001g0080 others(10): Show |
13 | HG01175.hp1 HG01433.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.704-4099dupG | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31676475 | |||||||
| chr12:31676512 | T | C | 362 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(359): Show |
410 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(407): Show |
intron_variant | MODIFIER | c.704-4135A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31676512 | |||||||
| chr12:31676524 | A | G | 1 | a0001c0001t0001g0329 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.704-4147T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31676524 | |||||||
| chr12:31676529 | A | G | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0002g0007 |
3 | HG01167.hp2 HG01169.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.704-4152T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31676529 | |||||||
| chr12:31676568 | C | T | 5 | a0001c0001t0001g0052 a0001c0001t0001g0060 a0001c0001t0001g0070 others(2): Show |
5 | HG00733.hp2 HG01081.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-4191G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31676568 | |||||||
| chr12:31676591 | C | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0135 a0001c0001t0001g0144 others(3): Show |
7 | HG02055.hp2 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.704-4214G>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31676591 | |||||||
| chr12:31676592 | A | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0135 a0001c0001t0001g0144 others(3): Show |
7 | HG02055.hp2 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.704-4215T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31676592 | |||||||
| chr12:31676612 | G | A | 2 | a0001c0001t0001g0324 a0001c0001t0001g0333 |
2 | HG03239.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.704-4235C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31676612 | |||||||
| chr12:31676630 | C | T | 1 | a0001c0001t0003g0085 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.704-4253G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31676630 | |||||||
| chr12:31676806 | T | G | 6 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(3): Show |
6 | HG01346.hp1 HG02683.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-4429A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31676806 | |||||||
| chr12:31676855 | A | G | 1 | a0001c0001t0001g0366 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.704-4478T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31676855 | |||||||
| chr12:31676936 | A | G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0181 a0001c0001t0001g0193 |
3 | HG02622.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.704-4559T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31676936 | |||||||
| chr12:31677028 | G | A | 49 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(46): Show |
51 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.704-4651C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31677028 | |||||||
| chr12:31677065 | G | A | 1 | a0001c0001t0006g0015 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.704-4688C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31677065 | |||||||
| chr12:31677095 | G | A | 75 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(72): Show |
80 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.704-4718C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31677095 | |||||||
| chr12:31677126 | G | A | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-4749C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31677126 | |||||||
| chr12:31677134 | TA | T | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-4758delT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31677134 | |||||||
| chr12:31677182 | C | A | 1 | a0001c0001t0001g0286 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.704-4805G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31677182 | |||||||
| chr12:31677249 | G | A | 1 | a0001c0001t0003g0378 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.704-4872C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31677249 | |||||||
| chr12:31677312 | A | C | 1 | a0001c0001t0002g0248 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.704-4935T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31677312 | |||||||
| chr12:31677325 | A | G | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-4948T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31677325 | |||||||
| chr12:31677432 | C | T | 1 | a0001c0001t0002g0189 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.704-5055G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31677432 | |||||||
| chr12:31677565 | T | C | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-5188A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31677565 | |||||||
| chr12:31677669 | T | TGGAAGGC others(4): Show |
1 | a0001c0001t0001g0065 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.704-5303_704-5293d others(13): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31677669 | |||||||
| chr12:31677717 | T | G | 4 | a0001c0001t0002g0155 a0001c0001t0002g0165 a0001c0001t0002g0172 others(1): Show |
4 | HG02572.hp1 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-5340A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31677717 | |||||||
| chr12:31677981 | A | G | 1 | a0001c0001t0001g0314 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.704-5604T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31677981 | |||||||
| chr12:31678035 | T | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0024 others(21): Show |
36 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.704-5658A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678035 | |||||||
| chr12:31678038 | T | C | 3 | a0001c0001t0001g0156 a0001c0001t0001g0181 a0001c0001t0001g0193 |
3 | HG02622.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.704-5661A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678038 | |||||||
| chr12:31678070 | A | G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0181 a0001c0001t0001g0193 |
3 | HG02622.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.704-5693T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678070 | |||||||
| chr12:31678145 | T | C | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
4 | HG01496.hp2 HG02300.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-5768A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678145 | |||||||
| chr12:31678221 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.704-5844A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678221 | |||||||
| chr12:31678362 | CAAG | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0263 |
3 | NA18969.hp1 NA18994.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.704-5988_704-5986d others(5): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678362 | |||||||
| chr12:31678394 | CT | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(274): Show |
317 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.704-6018delA | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678394 | |||||||
| chr12:31678394 | CTT | C | 10 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(7): Show |
10 | HG01496.hp2 HG02300.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.704-6019_704-6018d others(4): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678394 | |||||||
| chr12:31678418 | A | G | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-6041T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678418 | |||||||
| chr12:31678430 | C | T | 369 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(366): Show |
417 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(414): Show |
intron_variant | MODIFIER | c.704-6053G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678430 | |||||||
| chr12:31678449 | T | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0088 |
2 | HG01109.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.704-6072A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678449 | |||||||
| chr12:31678461 | A | G | 26 | a0001c0001t0001g0115 a0001c0001t0002g0019 a0001c0001t0002g0020 others(23): Show |
27 | HG00280.hp1 HG00408.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.704-6084T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678461 | |||||||
| chr12:31678483 | G | A | 1 | a0001c0001t0003g0102 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.704-6106C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678483 | |||||||
| chr12:31678506 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.704-6129G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678506 | |||||||
| chr12:31678555 | C | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(68): Show |
76 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.704-6178G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678555 | |||||||
| chr12:31678569 | G | C | 1 | a0001c0001t0001g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.704-6192C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678569 | |||||||
| chr12:31678689 | T | C | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.704-6312A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678689 | |||||||
| chr12:31678740 | A | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0024 others(21): Show |
36 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.704-6363T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678740 | |||||||
| chr12:31678744 | G | A | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.704-6367C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678744 | |||||||
| chr12:31678767 | G | T | 377 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(374): Show |
425 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(422): Show |
intron_variant | MODIFIER | c.704-6390C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678767 | |||||||
| chr12:31678920 | T | C | 3 | a0001c0001t0006g0015 a0001c0001t0006g0100 a0001c0001t0006g0101 |
4 | HG01943.hp2 HG01975.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-6543A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31678920 | |||||||
| chr12:31679136 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.704-6759G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31679136 | |||||||
| chr12:31679359 | T | A | 1 | a0001c0001t0005g0374 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.704-6982A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31679359 | |||||||
| chr12:31679460 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.704-7083C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31679460 | |||||||
| chr12:31679610 | C | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(204): Show |
242 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.704-7233G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31679610 | |||||||
| chr12:31679746 | T | A | 4 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-7369A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31679746 | |||||||
| chr12:31679750 | T | C | 1 | a0001c0001t0003g0045 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.704-7373A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31679750 | |||||||
| chr12:31679956 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.704-7579G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31679956 | |||||||
| chr12:31680038 | G | A | 1 | a0001c0004t0002g0383 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.704-7661C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680038 | |||||||
| chr12:31680042 | G | C | 73 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(70): Show |
78 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.704-7665C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680042 | |||||||
| chr12:31680048 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.704-7671C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680048 | |||||||
| chr12:31680077 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.704-7700G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680077 | |||||||
| chr12:31680078 | G | A | 5 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(2): Show |
5 | HG01496.hp2 HG02300.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-7701C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680078 | |||||||
| chr12:31680095 | G | C | 82 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(79): Show |
87 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.704-7718C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680095 | |||||||
| chr12:31680096 | C | CTG | 82 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(79): Show |
87 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.704-7720_704-7719i others(4): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680096 | |||||||
| chr12:31680102 | C | A | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.704-7725G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680102 | |||||||
| chr12:31680122 | C | CA | 79 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(76): Show |
84 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.704-7746dupT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680122 | |||||||
| chr12:31680182 | T | TA | 49 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
61 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.704-7806dupT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680182 | |||||||
| chr12:31680192 | A | ATTTTC | 4 | a0001c0001t0001g0305 a0001c0001t0001g0308 a0001c0001t0001g0309 others(1): Show |
4 | NA18942.hp1 NA18944.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-7820_704-7816d others(7): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680192 | |||||||
| chr12:31680192 | ATTTTC | A | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-7820_704-7816d others(7): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680192 | |||||||
| chr12:31680286 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.704-7909G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680286 | |||||||
| chr12:31680294 | G | A | 9 | a0001c0001t0002g0016 a0001c0001t0002g0116 a0001c0001t0002g0117 others(6): Show |
10 | HG02451.hp2 HG02723.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.704-7917C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680294 | |||||||
| chr12:31680416 | G | T | 2 | a0001c0001t0001g0292 a0001c0001t0001g0297 |
2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.704-8039C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680416 | |||||||
| chr12:31680456 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0046 a0001c0001t0001g0047 others(6): Show |
11 | HG00642.hp1 HG01099.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.704-8079G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680456 | |||||||
| chr12:31680502 | A | C | 65 | a0001c0001t0001g0115 a0001c0001t0002g0007 a0001c0001t0002g0013 others(62): Show |
71 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.704-8125T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680502 | |||||||
| chr12:31680518 | T | G | 53 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(50): Show |
55 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.704-8141A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680518 | |||||||
| chr12:31680632 | T | TAAGAAAT others(324): Show |
1 | a0001c0001t0001g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.704-8256_704-8255i others(333): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680632 | |||||||
| chr12:31680639 | T | C | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-8262A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680639 | |||||||
| chr12:31680682 | C | CAGGAGAT others(53): Show |
1 | a0001c0001t0001g0340 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.703+8265_704-8306d others(62): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680682 | |||||||
| chr12:31680881 | C | T | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
4 | HG02683.hp1 HG03710.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+8126G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680881 | |||||||
| chr12:31680943 | T | A | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+8064A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680943 | |||||||
| chr12:31680979 | T | G | 68 | a0001c0001t0001g0115 a0001c0001t0002g0007 a0001c0001t0002g0013 others(65): Show |
74 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.703+8028A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31680979 | |||||||
| chr12:31681055 | G | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+7952C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31681055 | |||||||
| chr12:31681250 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.703+7757G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31681250 | |||||||
| chr12:31681251 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0359 |
3 | HG01123.hp1 HG01175.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.703+7756C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31681251 | |||||||
| chr12:31681420 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0181 a0001c0001t0001g0193 |
3 | HG02622.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.703+7587C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31681420 | |||||||
| chr12:31681480 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.703+7527G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31681480 | |||||||
| chr12:31681509 | G | T | 1 | a0001c0001t0001g0249 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.703+7498C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31681509 | |||||||
| chr12:31681582 | T | C | 1 | a0001c0001t0005g0373 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.703+7425A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31681582 | |||||||
| chr12:31681597 | C | T | 1 | a0001c0001t0003g0091 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.703+7410G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31681597 | |||||||
| chr12:31681660 | C | T | 288 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
328 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.703+7347G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31681660 | |||||||
| chr12:31681914 | C | T | 1 | a0001c0001t0004g0237 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.703+7093G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31681914 | |||||||
| chr12:31681966 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.703+7041G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31681966 | |||||||
| chr12:31682398 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.703+6609C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31682398 | |||||||
| chr12:31682407 | A | C | 1 | a0002c0003t0001g0282 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.703+6600T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31682407 | |||||||
| chr12:31682449 | T | C | 61 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(58): Show |
66 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.703+6558A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31682449 | |||||||
| chr12:31682451 | C | G | 1 | a0001c0001t0008g0353 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.703+6556G>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31682451 | |||||||
| chr12:31682508 | C | T | 54 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(51): Show |
56 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.703+6499G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31682508 | |||||||
| chr12:31682515 | G | GGT | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+6490_703+6491d others(4): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31682515 | |||||||
| chr12:31682913 | C | T | 1 | a0001c0001t0001g0363 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.703+6094G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31682913 | |||||||
| chr12:31682958 | C | T | 54 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(51): Show |
56 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.703+6049G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31682958 | |||||||
| chr12:31682963 | C | CT | 51 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(48): Show |
63 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.703+6043dupA | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31682963 | |||||||
| chr12:31682963 | C | CTT | 73 | a0001c0001t0001g0115 a0001c0001t0001g0234 a0001c0001t0002g0007 others(70): Show |
79 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.703+6042_703+6043d others(4): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31682963 | |||||||
| chr12:31682963 | CT | C | 15 | a0001c0001t0001g0065 a0001c0001t0001g0249 a0001c0001t0001g0314 others(12): Show |
15 | HG00323.hp1 HG02559.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.703+6043delA | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31682963 | |||||||
| chr12:31683218 | C | T | 1 | a0001c0001t0001g0340 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.703+5789G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31683218 | |||||||
| chr12:31683219 | T | C | 1 | a0001c0001t0001g0340 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.703+5788A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31683219 | |||||||
| chr12:31683220 | C | A | 1 | a0001c0001t0001g0340 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.703+5787G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31683220 | |||||||
| chr12:31683252 | A | G | 377 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(374): Show |
425 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(422): Show |
intron_variant | MODIFIER | c.703+5755T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31683252 | |||||||
| chr12:31683406 | C | T | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+5601G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31683406 | |||||||
| chr12:31683463 | G | A | 50 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
62 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.703+5544C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31683463 | |||||||
| chr12:31683577 | A | G | 1 | a0001c0001t0003g0095 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.703+5430T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31683577 | |||||||
| chr12:31683580 | GTAAA | G | 3 | a0001c0001t0002g0128 a0001c0001t0002g0146 a0001c0001t0002g0162 |
3 | HG00280.hp1 HG01123.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.703+5423_703+5426d others(6): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31683580 | |||||||
| chr12:31683585 | T | A | 1 | a0001c0001t0001g0340 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.703+5422A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31683585 | |||||||
| chr12:31683586 | A | T | 1 | a0001c0001t0001g0340 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.703+5421T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31683586 | |||||||
| chr12:31683668 | C | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0276 a0001c0001t0001g0279 others(4): Show |
10 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.703+5339G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31683668 | |||||||
| chr12:31683678 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.703+5329C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31683678 | |||||||
| chr12:31683955 | C | T | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+5052G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31683955 | |||||||
| chr12:31683976 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.703+5031C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31683976 | |||||||
| chr12:31684012 | T | C | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+4995A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31684012 | |||||||
| chr12:31684016 | G | A | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
327 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.703+4991C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31684016 | |||||||
| chr12:31684017 | T | A | 1 | a0001c0001t0001g0340 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.703+4990A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31684017 | |||||||
| chr12:31684097 | C | T | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+4910G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31684097 | |||||||
| chr12:31684180 | C | T | 1 | a0001c0001t0006g0100 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.703+4827G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31684180 | |||||||
| chr12:31684216 | C | A | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+4791G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31684216 | |||||||
| chr12:31684314 | G | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+4693C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31684314 | |||||||
| chr12:31684337 | T | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+4670A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31684337 | |||||||
| chr12:31684393 | T | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+4614A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31684393 | |||||||
| chr12:31684396 | T | TA | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+4610dupT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31684396 | |||||||
| chr12:31684447 | A | G | 1 | a0001c0001t0002g0128 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.703+4560T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31684447 | |||||||
| chr12:31684472 | A | AT | 9 | a0001c0001t0001g0087 a0001c0001t0001g0138 a0001c0001t0001g0139 others(6): Show |
9 | HG01496.hp2 HG02300.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.703+4534dupA | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31684472 | |||||||
| chr12:31684498 | T | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+4509A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31684498 | |||||||
| chr12:31684616 | G | A | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+4391C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31684616 | |||||||
| chr12:31684673 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0011 others(57): Show |
78 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.703+4334C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31684673 | |||||||
| chr12:31684720 | C | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
61 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.703+4287G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31684720 | |||||||
| chr12:31684750 | C | T | 25 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(22): Show |
25 | HG00438.hp2 HG02027.hp2 HG02129.hp1 others(22): Show |
intron_variant | MODIFIER | c.703+4257G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31684750 | |||||||
| chr12:31684777 | C | A | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+4230G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31684777 | |||||||
| chr12:31684969 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.703+4038C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31684969 | |||||||
| chr12:31685027 | T | TG | 13 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0087 others(10): Show |
13 | HG00735.hp2 HG01106.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.703+3979_703+3980i others(3): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685027 | |||||||
| chr12:31685028 | A | AT | 3 | a0001c0001t0001g0156 a0001c0001t0001g0181 a0001c0001t0001g0193 |
3 | HG02622.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.703+3978dupA | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685028 | |||||||
| chr12:31685028 | A | G | 355 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(352): Show |
403 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.703+3979T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685028 | |||||||
| chr12:31685028 | A | T | 14 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0087 others(11): Show |
14 | HG00735.hp2 HG01106.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.703+3979T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685028 | |||||||
| chr12:31685030 | TA | T | 19 | a0001c0001t0001g0246 a0001c0001t0002g0112 a0001c0001t0002g0161 others(16): Show |
20 | HG00733.hp1 HG01928.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.703+3976delT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685030 | |||||||
| chr12:31685031 | A | T | 363 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(360): Show |
410 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(407): Show |
intron_variant | MODIFIER | c.703+3976T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685031 | |||||||
| chr12:31685040 | T | G | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+3967A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685040 | |||||||
| chr12:31685077 | G | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
61 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.703+3930C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685077 | |||||||
| chr12:31685088 | C | A | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
328 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.703+3919G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685088 | |||||||
| chr12:31685164 | G | A | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+3843C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685164 | |||||||
| chr12:31685166 | T | C | 4 | a0001c0001t0002g0379 a0001c0001t0002g0380 a0001c0001t0002g0381 others(1): Show |
4 | HG02451.hp2 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+3841A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685166 | |||||||
| chr12:31685257 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.703+3750C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685257 | |||||||
| chr12:31685274 | C | T | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+3733G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685274 | |||||||
| chr12:31685295 | T | C | 2 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.703+3712A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685295 | |||||||
| chr12:31685308 | C | A | 1 | a0001c0001t0003g0114 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.703+3699G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685308 | |||||||
| chr12:31685349 | T | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+3658A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685349 | |||||||
| chr12:31685526 | C | T | 2 | a0001c0002t0007g0274 a0001c0002t0007g0275 |
2 | HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.703+3481G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685526 | |||||||
| chr12:31685535 | T | G | 1 | a0001c0001t0001g0340 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.703+3472A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685535 | |||||||
| chr12:31685564 | G | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(100): Show |
117 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.703+3443C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685564 | |||||||
| chr12:31685602 | A | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+3405T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685602 | |||||||
| chr12:31685658 | A | G | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+3349T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685658 | |||||||
| chr12:31685659 | G | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0088 |
2 | HG01109.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.703+3348C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685659 | |||||||
| chr12:31685670 | G | A | 2 | a0001c0001t0001g0354 a0001c0001t0001g0355 |
2 | NA18982.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.703+3337C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685670 | |||||||
| chr12:31685674 | G | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+3333C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685674 | |||||||
| chr12:31685708 | G | T | 1 | a0001c0001t0001g0071 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.703+3299C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685708 | |||||||
| chr12:31685733 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.703+3274C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685733 | |||||||
| chr12:31685800 | C | CAAAAAA | 9 | a0001c0001t0001g0056 a0001c0001t0001g0089 a0001c0001t0001g0219 others(6): Show |
9 | HG01070.hp1 HG01169.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+3201_703+3206d others(8): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685800 | |||||||
| chr12:31685800 | C | CAAAAAAA | 265 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(262): Show |
299 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.703+3200_703+3206d others(9): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685800 | |||||||
| chr12:31685800 | C | CAAAAAAA others(1): Show |
58 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(55): Show |
60 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.703+3199_703+3206d others(10): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685800 | |||||||
| chr12:31685800 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0123 a0001c0001t0001g0125 |
2 | HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.703+3197_703+3206d others(12): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685800 | |||||||
| chr12:31685807 | A | AAAAAAAA others(4): Show |
5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+3199_703+3200i others(13): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685807 | |||||||
| chr12:31685807 | A | AAAAAAAG | 30 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0024 others(27): Show |
42 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.703+3199_703+3200i others(9): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685807 | |||||||
| chr12:31685823 | G | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+3184C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685823 | |||||||
| chr12:31685829 | A | G | 1 | a0001c0001t0002g0155 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.703+3178T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685829 | |||||||
| chr12:31685836 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | NA19004.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.703+3171G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685836 | |||||||
| chr12:31685843 | G | A | 68 | a0001c0001t0001g0115 a0001c0001t0002g0007 a0001c0001t0002g0013 others(65): Show |
74 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.703+3164C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685843 | |||||||
| chr12:31685855 | A | AT | 67 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(64): Show |
73 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.703+3151dupA | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685855 | |||||||
| chr12:31685855 | A | T | 3 | a0001c0001t0001g0326 a0001c0001t0001g0337 a0001c0001t0001g0342 |
3 | HG00558.hp1 NA18977.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.703+3152T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685855 | |||||||
| chr12:31685855 | AT | A | 12 | a0001c0001t0001g0056 a0001c0001t0001g0138 a0001c0001t0001g0139 others(9): Show |
12 | HG01496.hp2 HG02135.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.703+3151delA | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685855 | |||||||
| chr12:31685858 | T | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
61 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.703+3149A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685858 | |||||||
| chr12:31685889 | G | T | 5 | a0001c0001t0002g0016 a0001c0001t0002g0116 a0001c0001t0002g0117 others(2): Show |
6 | HG02723.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.703+3118C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685889 | |||||||
| chr12:31685946 | A | G | 5 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(2): Show |
5 | HG01496.hp2 HG02300.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+3061T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31685946 | |||||||
| chr12:31686218 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.703+2789C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31686218 | |||||||
| chr12:31686227 | C | A | 1 | a0001c0001t0001g0340 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.703+2780G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31686227 | |||||||
| chr12:31686530 | C | CATT | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+2476_703+2477i others(5): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31686530 | |||||||
| chr12:31686653 | C | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(21): Show |
29 | HG00735.hp1 HG01928.hp2 HG01993.hp2 others(26): Show |
intron_variant | MODIFIER | c.703+2354G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31686653 | |||||||
| chr12:31686713 | T | C | 1 | a0001c0001t0002g0172 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.703+2294A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31686713 | |||||||
| chr12:31686735 | T | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+2272A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31686735 | |||||||
| chr12:31686759 | T | C | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+2248A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31686759 | |||||||
| chr12:31686839 | T | C | 4 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+2168A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31686839 | |||||||
| chr12:31686977 | C | G | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+2030G>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31686977 | |||||||
| chr12:31687035 | G | C | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+1972C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31687035 | |||||||
| chr12:31687171 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.703+1836G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31687171 | |||||||
| chr12:31687281 | C | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0024 others(21): Show |
36 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.703+1726G>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31687281 | |||||||
| chr12:31687320 | T | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+1687A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31687320 | |||||||
| chr12:31687368 | T | C | 1 | a0001c0001t0002g0163 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.703+1639A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31687368 | |||||||
| chr12:31687529 | A | G | 2 | a0001c0002t0007g0274 a0001c0002t0007g0275 |
2 | HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.703+1478T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31687529 | |||||||
| chr12:31687662 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.703+1345C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31687662 | |||||||
| chr12:31687685 | T | C | 36 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0090 others(33): Show |
42 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.703+1322A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31687685 | |||||||
| chr12:31687686 | C | CA | 11 | a0001c0001t0001g0017 a0001c0001t0001g0044 a0001c0001t0001g0144 others(8): Show |
12 | HG02055.hp2 HG02559.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.703+1320dupT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31687686 | |||||||
| chr12:31687756 | G | T | 1 | a0001c0001t0003g0083 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.703+1251C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31687756 | |||||||
| chr12:31687793 | A | G | 36 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0090 others(33): Show |
42 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.703+1214T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31687793 | |||||||
| chr12:31687893 | C | T | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+1114G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31687893 | |||||||
| chr12:31688015 | C | T | 3 | a0001c0001t0001g0262 a0001c0001t0001g0306 a0001c0001t0001g0311 |
3 | NA18972.hp1 NA18983.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.703+992G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31688015 | |||||||
| chr12:31688065 | C | T | 1 | a0001c0001t0001g0367 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.703+942G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31688065 | |||||||
| chr12:31688077 | C | G | 1 | a0001c0001t0001g0249 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.703+930G>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31688077 | |||||||
| chr12:31688112 | A | G | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+895T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31688112 | |||||||
| chr12:31688181 | C | T | 69 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(66): Show |
74 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.703+826G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31688181 | |||||||
| chr12:31688200 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.703+807G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31688200 | |||||||
| chr12:31688236 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.703+771C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31688236 | |||||||
| chr12:31688245 | C | T | 6 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0001c0001t0004g0055 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+762G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31688245 | |||||||
| chr12:31688386 | T | C | 369 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(366): Show |
417 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(414): Show |
intron_variant | MODIFIER | c.703+621A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31688386 | |||||||
| chr12:31688442 | T | C | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+565A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31688442 | |||||||
| chr12:31688582 | C | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+425G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31688582 | |||||||
| chr12:31688593 | A | T | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+414T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31688593 | |||||||
| chr12:31688604 | T | TA | 72 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(69): Show |
77 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.703+402dupT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31688604 | |||||||
| chr12:31688685 | C | A | 7 | a0001c0001t0001g0350 a0001c0001t0001g0351 a0001c0001t0001g0352 others(4): Show |
7 | HG02155.hp1 NA18978.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.703+322G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31688685 | |||||||
| chr12:31688787 | G | A | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+220C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31688787 | |||||||
| chr12:31688796 | G | A | 1 | a0001c0001t0002g0020 | 2 | HG00408.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.703+211C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31688796 | |||||||
| chr12:31688819 | T | TTAAAA | 36 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0090 others(33): Show |
42 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.703+183_703+187dup others(5): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 6/6 | chr12 | 31688819 | |||||||
| chr12:31689478 | G | A | 3 | a0001c0001t0003g0091 a0001c0001t0003g0092 a0001c0001t0003g0093 |
3 | NA18974.hp2 NA19062.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.592-360C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31689478 | |||||||
| chr12:31689492 | T | C | 1 | a0001c0001t0001g0370 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.592-374A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31689492 | |||||||
| chr12:31689507 | T | TA | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-390dupT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31689507 | |||||||
| chr12:31689546 | C | T | 3 | a0001c0001t0003g0095 a0001c0001t0003g0097 a0001c0001t0003g0105 |
3 | HG00735.hp2 NA20300.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.592-428G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31689546 | |||||||
| chr12:31689583 | T | C | 9 | a0001c0001t0002g0016 a0001c0001t0002g0116 a0001c0001t0002g0117 others(6): Show |
10 | HG02451.hp2 HG02723.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.592-465A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31689583 | |||||||
| chr12:31689619 | T | C | 3 | a0001c0001t0001g0156 a0001c0001t0001g0181 a0001c0001t0001g0193 |
3 | HG02622.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.592-501A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31689619 | |||||||
| chr12:31689663 | A | T | 64 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(61): Show |
69 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.592-545T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31689663 | |||||||
| chr12:31689669 | A | G | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.592-551T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31689669 | |||||||
| chr12:31689764 | T | A | 2 | a0001c0001t0004g0054 a0001c0001t0004g0110 |
2 | HG01884.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.592-646A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31689764 | |||||||
| chr12:31689765 | A | T | 1 | a0001c0001t0001g0286 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.592-647T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31689765 | |||||||
| chr12:31689779 | A | G | 369 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(366): Show |
417 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(414): Show |
intron_variant | MODIFIER | c.592-661T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31689779 | |||||||
| chr12:31689845 | G | C | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-727C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31689845 | |||||||
| chr12:31689846 | G | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0147 a0001c0001t0001g0148 |
4 | HG02055.hp2 HG02965.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-728C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31689846 | |||||||
| chr12:31689917 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.592-799G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31689917 | |||||||
| chr12:31689923 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.592-805G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31689923 | |||||||
| chr12:31689936 | A | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-818T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31689936 | |||||||
| chr12:31689942 | A | G | 1 | a0001c0001t0001g0358 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.592-824T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31689942 | |||||||
| chr12:31690001 | C | T | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-883G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31690001 | |||||||
| chr12:31690102 | TGG | T | 9 | a0001c0001t0002g0016 a0001c0001t0002g0116 a0001c0001t0002g0117 others(6): Show |
10 | HG02451.hp2 HG02723.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.592-986_592-985del others(2): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31690102 | |||||||
| chr12:31690179 | T | G | 5 | a0001c0001t0002g0016 a0001c0001t0002g0116 a0001c0001t0002g0117 others(2): Show |
6 | HG02723.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.592-1061A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31690179 | |||||||
| chr12:31690241 | G | A | 1 | a0001c0001t0004g0110 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.592-1123C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31690241 | |||||||
| chr12:31690322 | A | G | 78 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(75): Show |
83 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.592-1204T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31690322 | |||||||
| chr12:31690329 | C | A | 1 | a0001c0001t0001g0234 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.592-1211G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31690329 | |||||||
| chr12:31690472 | C | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0024 others(20): Show |
34 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.592-1354G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31690472 | |||||||
| chr12:31690499 | G | A | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.592-1381C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31690499 | |||||||
| chr12:31690506 | C | T | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.592-1388G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31690506 | |||||||
| chr12:31690642 | A | G | 4 | a0001c0001t0001g0156 a0001c0001t0001g0181 a0001c0001t0001g0193 others(1): Show |
4 | HG01167.hp1 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-1524T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31690642 | |||||||
| chr12:31690952 | G | A | 9 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.592-1834C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31690952 | |||||||
| chr12:31691137 | CA | C | 332 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(329): Show |
374 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.592-2020delT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31691137 | |||||||
| chr12:31691137 | CAA | C | 9 | a0001c0001t0001g0142 a0001c0001t0001g0224 a0001c0001t0001g0280 others(6): Show |
9 | HG00558.hp1 HG01256.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.592-2021_592-2020d others(4): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31691137 | |||||||
| chr12:31691245 | T | G | 64 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(61): Show |
69 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.592-2127A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31691245 | |||||||
| chr12:31691452 | T | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0059 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.592-2334A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31691452 | |||||||
| chr12:31691581 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.592-2463T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31691581 | |||||||
| chr12:31691789 | A | G | 1 | a0001c0001t0001g0362 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.592-2671T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31691789 | |||||||
| chr12:31691843 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
127 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.592-2725C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31691843 | |||||||
| chr12:31691887 | AT | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-2770delA | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31691887 | |||||||
| chr12:31691946 | T | C | 377 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(374): Show |
425 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(422): Show |
intron_variant | MODIFIER | c.592-2828A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31691946 | |||||||
| chr12:31691985 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
330 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.592-2867A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31691985 | |||||||
| chr12:31692003 | A | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-2885T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31692003 | |||||||
| chr12:31692062 | G | C | 1 | a0001c0001t0002g0183 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.592-2944C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31692062 | |||||||
| chr12:31692160 | A | C | 68 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(65): Show |
73 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.592-3042T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31692160 | |||||||
| chr12:31692197 | G | T | 1 | a0001c0001t0001g0370 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.592-3079C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31692197 | |||||||
| chr12:31692328 | G | C | 1 | a0001c0001t0001g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.592-3210C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31692328 | |||||||
| chr12:31692340 | C | T | 1 | a0001c0001t0003g0094 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.592-3222G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31692340 | |||||||
| chr12:31692349 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.592-3231A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31692349 | |||||||
| chr12:31692351 | G | A | 4 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-3233C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31692351 | |||||||
| chr12:31692382 | G | A | 35 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0106 others(32): Show |
41 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.592-3264C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31692382 | |||||||
| chr12:31692449 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.592-3331G>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31692449 | |||||||
| chr12:31692451 | CA | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(174): Show |
201 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.592-3334delT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31692451 | |||||||
| chr12:31692460 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.592-3342T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31692460 | |||||||
| chr12:31692477 | AC | A | 5 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(2): Show |
5 | HG01496.hp2 HG02300.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.592-3360delG | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31692477 | |||||||
| chr12:31692536 | G | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-3418C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31692536 | |||||||
| chr12:31692647 | G | A | 49 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(46): Show |
51 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.592-3529C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31692647 | |||||||
| chr12:31692723 | T | C | 1 | a0001c0001t0003g0097 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.592-3605A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31692723 | |||||||
| chr12:31692730 | C | CAAGTA | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-3617_592-3613d others(7): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31692730 | |||||||
| chr12:31692748 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.592-3630G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31692748 | |||||||
| chr12:31693002 | C | T | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-3884G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31693002 | |||||||
| chr12:31693026 | G | A | 49 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(46): Show |
51 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.592-3908C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31693026 | |||||||
| chr12:31693040 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.592-3922A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31693040 | |||||||
| chr12:31693058 | C | CT | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-3941dupA | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31693058 | |||||||
| chr12:31693094 | G | A | 1 | a0001c0001t0002g0182 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.592-3976C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31693094 | |||||||
| chr12:31693105 | G | T | 73 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(70): Show |
78 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.592-3987C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31693105 | |||||||
| chr12:31693187 | C | T | 6 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0001c0001t0004g0055 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.592-4069G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31693187 | |||||||
| chr12:31693282 | G | T | 1 | a0001c0001t0001g0377 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.591+4079C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31693282 | |||||||
| chr12:31693299 | G | A | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
4 | HG01496.hp2 HG02300.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.591+4062C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31693299 | |||||||
| chr12:31693414 | T | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+3947A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31693414 | |||||||
| chr12:31693476 | C | T | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+3885G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31693476 | |||||||
| chr12:31693524 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.591+3837C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31693524 | |||||||
| chr12:31693794 | A | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.591+3567T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31693794 | |||||||
| chr12:31693832 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0147 a0001c0001t0001g0148 |
4 | HG02055.hp2 HG02965.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+3529C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31693832 | |||||||
| chr12:31693853 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.591+3508A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31693853 | |||||||
| chr12:31693889 | T | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+3472A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31693889 | |||||||
| chr12:31694072 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0046 a0001c0001t0001g0047 others(6): Show |
11 | HG00642.hp1 HG01099.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.591+3289G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31694072 | |||||||
| chr12:31694116 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.591+3245G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31694116 | |||||||
| chr12:31694140 | T | TA | 75 | a0001c0001t0001g0115 a0001c0001t0002g0007 a0001c0001t0002g0013 others(72): Show |
82 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.591+3220dupT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31694140 | |||||||
| chr12:31694234 | G | T | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
4 | HG01496.hp2 HG02300.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.591+3127C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31694234 | |||||||
| chr12:31694292 | A | C | 24 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(21): Show |
24 | HG00438.hp2 HG02027.hp2 HG02129.hp1 others(21): Show |
intron_variant | MODIFIER | c.591+3069T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31694292 | |||||||
| chr12:31694319 | A | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+3042T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31694319 | |||||||
| chr12:31694405 | G | A | 1 | a0001c0001t0002g0380 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.591+2956C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31694405 | |||||||
| chr12:31694442 | C | CA | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(145): Show |
162 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.591+2918dupT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31694442 | |||||||
| chr12:31694442 | C | CAA | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(127): Show |
156 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.591+2917_591+2918d others(4): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31694442 | |||||||
| chr12:31694442 | C | CAAA | 8 | a0001c0001t0001g0126 a0001c0001t0001g0138 a0001c0001t0001g0142 others(5): Show |
8 | HG02300.hp2 HG03942.hp2 HG04228.hp2 others(5): Show |
intron_variant | MODIFIER | c.591+2916_591+2918d others(5): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31694442 | |||||||
| chr12:31694442 | CA | C | 6 | a0001c0001t0002g0160 a0001c0001t0002g0175 a0001c0001t0002g0177 others(3): Show |
6 | HG01975.hp1 HG02293.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+2918delT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31694442 | |||||||
| chr12:31694602 | C | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0181 a0001c0001t0001g0193 |
3 | HG02622.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.591+2759G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31694602 | |||||||
| chr12:31694620 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.591+2741G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31694620 | |||||||
| chr12:31694700 | T | C | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
336 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.591+2661A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31694700 | |||||||
| chr12:31694866 | A | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+2495T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31694866 | |||||||
| chr12:31694937 | T | TACAAA | 6 | a0001c0001t0001g0247 a0001c0001t0005g0371 a0001c0001t0005g0372 others(3): Show |
6 | HG02809.hp2 HG02922.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.591+2419_591+2423d others(7): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31694937 | |||||||
| chr12:31695102 | T | C | 24 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(21): Show |
24 | HG00438.hp2 HG02027.hp2 HG02129.hp1 others(21): Show |
intron_variant | MODIFIER | c.591+2259A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31695102 | |||||||
| chr12:31695213 | T | C | 50 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
62 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.591+2148A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31695213 | |||||||
| chr12:31695413 | T | C | 377 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(374): Show |
425 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(422): Show |
intron_variant | MODIFIER | c.591+1948A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31695413 | |||||||
| chr12:31695457 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.591+1904A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31695457 | |||||||
| chr12:31695458 | A | C | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.591+1903T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31695458 | |||||||
| chr12:31695466 | T | C | 1 | a0001c0001t0001g0370 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.591+1895A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31695466 | |||||||
| chr12:31695471 | A | ATTTC | 83 | a0001c0001t0001g0115 a0001c0001t0001g0135 a0001c0001t0001g0136 others(80): Show |
90 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.591+1886_591+1889d others(6): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31695471 | |||||||
| chr12:31695487 | C | CTTTCT | 188 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(185): Show |
208 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.591+1873_591+1874i others(7): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31695487 | |||||||
| chr12:31695487 | C | CTTTCTT | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
123 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.591+1873_591+1874i others(8): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31695487 | |||||||
| chr12:31695487 | C | CTTTCTTT others(3): Show |
1 | a0001c0001t0003g0114 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.591+1873_591+1874i others(12): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31695487 | |||||||
| chr12:31695515 | G | A | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
4 | HG01496.hp2 HG02300.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.591+1846C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31695515 | |||||||
| chr12:31695537 | T | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+1824A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31695537 | |||||||
| chr12:31695599 | T | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+1762A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31695599 | |||||||
| chr12:31695617 | C | T | 1 | a0001c0001t0001g0307 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.591+1744G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31695617 | |||||||
| chr12:31695710 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.591+1651G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31695710 | |||||||
| chr12:31695733 | T | C | 50 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
62 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.591+1628A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31695733 | |||||||
| chr12:31695756 | G | A | 5 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0001c0001t0004g0055 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+1605C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31695756 | |||||||
| chr12:31695816 | A | T | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+1545T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31695816 | |||||||
| chr12:31696056 | A | T | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.591+1305T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31696056 | |||||||
| chr12:31696110 | G | T | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+1251C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31696110 | |||||||
| chr12:31696204 | T | TC | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
4 | HG01496.hp2 HG02300.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.591+1156dupG | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31696204 | |||||||
| chr12:31696250 | A | T | 111 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(108): Show |
117 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.591+1111T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31696250 | |||||||
| chr12:31696254 | T | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0138 a0001c0001t0001g0139 others(6): Show |
10 | HG01496.hp2 HG02055.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.591+1107A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31696254 | |||||||
| chr12:31696280 | G | GTATT | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0173 |
3 | HG00140.hp2 HG01433.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.591+1077_591+1080d others(6): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31696280 | |||||||
| chr12:31696280 | G | GTATTTAT others(1): Show |
299 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(296): Show |
342 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.591+1073_591+1080d others(10): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31696280 | |||||||
| chr12:31696280 | G | GTATTTAT others(5): Show |
61 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0090 others(58): Show |
66 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.591+1069_591+1080d others(14): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31696280 | |||||||
| chr12:31696280 | G | GTATTTAT others(9): Show |
16 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(13): Show |
16 | HG02027.hp2 NA18612.hp1 NA18948.hp1 others(13): Show |
intron_variant | MODIFIER | c.591+1080_591+1081i others(18): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31696280 | |||||||
| chr12:31696304 | T | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+1057A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31696304 | |||||||
| chr12:31696357 | T | G | 1 | a0001c0001t0001g0309 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.591+1004A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31696357 | |||||||
| chr12:31696744 | C | T | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
327 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.591+617G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31696744 | |||||||
| chr12:31696767 | A | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+594T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31696767 | |||||||
| chr12:31696783 | C | T | 1 | a0001c0001t0002g0180 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.591+578G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31696783 | |||||||
| chr12:31696907 | G | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+454C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31696907 | |||||||
| chr12:31696920 | C | CA | 13 | a0001c0001t0001g0080 a0001c0001t0001g0206 a0001c0001t0001g0216 others(10): Show |
13 | HG02071.hp2 HG02074.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+440dupT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31696920 | |||||||
| chr12:31697010 | G | A | 2 | a0001c0001t0003g0098 a0001c0001t0003g0104 |
2 | HG02074.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.591+351C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31697010 | |||||||
| chr12:31697130 | G | T | 369 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(366): Show |
417 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(414): Show |
intron_variant | MODIFIER | c.591+231C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31697130 | |||||||
| chr12:31697244 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.591+117T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31697244 | |||||||
| chr12:31697286 | C | T | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
327 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.591+75G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31697286 | |||||||
| chr12:31697349 | T | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0024 others(20): Show |
34 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.591+12A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 5/6 | chr12 | 31697349 | |||||||
| chr12:31697682 | A | T | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.534+58T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 4/6 | chr12 | 31697682 | |||||||
| chr12:31697974 | T | C | 6 | a0001c0001t0001g0023 a0001c0001t0001g0223 a0001c0001t0001g0235 others(3): Show |
7 | NA18947.hp2 NA18956.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-17A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31697974 | |||||||
| chr12:31698110 | A | G | 377 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(374): Show |
425 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(422): Show |
intron_variant | MODIFIER | c.317-153T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31698110 | |||||||
| chr12:31698161 | T | G | 45 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0036 others(42): Show |
48 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.317-204A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31698161 | |||||||
| chr12:31698207 | GA | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-251delT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31698207 | |||||||
| chr12:31698348 | T | C | 49 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
61 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.317-391A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31698348 | |||||||
| chr12:31698390 | G | T | 1 | a0001c0002t0007g0275 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.317-433C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31698390 | |||||||
| chr12:31698427 | C | T | 1 | a0001c0001t0001g0317 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.317-470G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31698427 | |||||||
| chr12:31698513 | C | A | 6 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0001c0001t0004g0055 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.317-556G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31698513 | |||||||
| chr12:31698518 | GGTCAAAA others(7): Show |
G | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.317-575_317-562del others(14): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31698518 | |||||||
| chr12:31698741 | C | CT | 49 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
61 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.317-785dupA | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31698741 | |||||||
| chr12:31698852 | C | T | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | NA18984.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.317-895G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31698852 | |||||||
| chr12:31699030 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.317-1073C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699030 | |||||||
| chr12:31699111 | A | C | 369 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(366): Show |
417 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(414): Show |
intron_variant | MODIFIER | c.317-1154T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699111 | |||||||
| chr12:31699193 | G | T | 50 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
62 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.317-1236C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699193 | |||||||
| chr12:31699284 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.317-1327G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699284 | |||||||
| chr12:31699395 | C | CA | 33 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0046 others(30): Show |
36 | HG00642.hp1 HG01069.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.317-1439dupT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699395 | |||||||
| chr12:31699395 | C | CAA | 93 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(90): Show |
112 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.317-1440_317-1439d others(4): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699395 | |||||||
| chr12:31699395 | C | CAAA | 52 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0042 others(49): Show |
53 | HG00609.hp1 HG00639.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.317-1441_317-1439d others(5): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699395 | |||||||
| chr12:31699395 | C | CAAAA | 57 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0001g0115 others(54): Show |
63 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.317-1442_317-1439d others(6): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699395 | |||||||
| chr12:31699395 | C | CAAAAA | 19 | a0001c0001t0002g0035 a0001c0001t0002g0134 a0001c0001t0002g0150 others(16): Show |
19 | HG00597.hp1 HG00673.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.317-1443_317-1439d others(7): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699395 | |||||||
| chr12:31699395 | C | CAAAAAA | 14 | a0001c0001t0001g0324 a0001c0001t0001g0330 a0001c0001t0001g0331 others(11): Show |
14 | HG00438.hp1 HG00609.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.317-1444_317-1439d others(8): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699395 | |||||||
| chr12:31699395 | C | CAAAAAAA | 20 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0323 others(17): Show |
21 | HG00323.hp1 HG00558.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.317-1445_317-1439d others(9): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699395 | |||||||
| chr12:31699395 | C | CAAAAAAA others(1): Show |
9 | a0001c0001t0001g0030 a0001c0001t0001g0332 a0001c0001t0001g0335 others(6): Show |
10 | HG01175.hp1 HG02040.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.317-1446_317-1439d others(10): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699395 | |||||||
| chr12:31699395 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0343 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.317-1448_317-1439d others(12): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699395 | |||||||
| chr12:31699395 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0344 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.317-1450_317-1439d others(14): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699395 | |||||||
| chr12:31699395 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0329 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.317-1451_317-1439d others(15): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699395 | |||||||
| chr12:31699395 | CA | C | 28 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0261 others(25): Show |
33 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.317-1439delT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699395 | |||||||
| chr12:31699395 | CAAAAAAA | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0024 others(18): Show |
32 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.317-1445_317-1439d others(9): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699395 | |||||||
| chr12:31699395 | CAAAAAAA others(7): Show |
C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-1452_317-1439d others(16): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699395 | |||||||
| chr12:31699566 | C | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
61 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.317-1609G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699566 | |||||||
| chr12:31699592 | C | A | 1 | a0001c0001t0001g0251 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.317-1635G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699592 | |||||||
| chr12:31699620 | T | C | 3 | a0001c0001t0001g0156 a0001c0001t0001g0181 a0001c0001t0001g0193 |
3 | HG02622.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.317-1663A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699620 | |||||||
| chr12:31699681 | A | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-1724T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699681 | |||||||
| chr12:31699743 | T | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0144 a0001c0001t0001g0145 others(2): Show |
6 | HG02055.hp2 HG02647.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.317-1786A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699743 | |||||||
| chr12:31699875 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.317-1918C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699875 | |||||||
| chr12:31699928 | A | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+1935T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699928 | |||||||
| chr12:31699962 | G | C | 6 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0001c0001t0004g0055 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.316+1901C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31699962 | |||||||
| chr12:31700149 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.316+1714A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31700149 | |||||||
| chr12:31700150 | AT | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+1712delA | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31700150 | |||||||
| chr12:31700153 | TA | T | 9 | a0001c0001t0001g0039 a0001c0001t0001g0225 a0001c0001t0001g0280 others(6): Show |
9 | HG01243.hp1 HG01256.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.316+1709delT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31700153 | |||||||
| chr12:31700242 | G | A | 4 | a0001c0001t0002g0112 a0001c0001t0006g0015 a0001c0001t0006g0100 others(1): Show |
5 | HG01943.hp2 HG01975.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+1621C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31700242 | |||||||
| chr12:31700435 | G | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.316+1428C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31700435 | |||||||
| chr12:31700815 | G | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+1048C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31700815 | |||||||
| chr12:31700911 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.316+952C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31700911 | |||||||
| chr12:31700924 | C | T | 65 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(62): Show |
70 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.316+939G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31700924 | |||||||
| chr12:31700964 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.316+899G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31700964 | |||||||
| chr12:31700968 | C | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+895G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31700968 | |||||||
| chr12:31700997 | G | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0024 others(21): Show |
36 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.316+866C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31700997 | |||||||
| chr12:31701156 | C | T | 28 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0106 others(25): Show |
34 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.316+707G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31701156 | |||||||
| chr12:31701330 | C | G | 68 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(65): Show |
73 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.316+533G>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31701330 | |||||||
| chr12:31701397 | G | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+466C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31701397 | |||||||
| chr12:31701406 | G | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+457C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31701406 | |||||||
| chr12:31701505 | C | T | 369 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(366): Show |
417 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(414): Show |
intron_variant | MODIFIER | c.316+358G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31701505 | |||||||
| chr12:31701655 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.316+208G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31701655 | |||||||
| chr12:31701785 | G | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.316+78C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 3/6 | chr12 | 31701785 | |||||||
| chr12:31702010 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02723.hp2 | splice_region_variant&intron_variant | LOW | c.172-3T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31702010 | |||||||
| chr12:31702049 | T | C | 1 | a0001c0001t0001g0370 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.172-42A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31702049 | |||||||
| chr12:31702243 | T | G | 1 | a0001c0001t0001g0370 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.172-236A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31702243 | |||||||
| chr12:31702373 | A | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-366T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31702373 | |||||||
| chr12:31702549 | T | TGTGA | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-543_172-542ins others(4): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31702549 | |||||||
| chr12:31702567 | A | T | 63 | a0001c0001t0001g0115 a0001c0001t0002g0007 a0001c0001t0002g0013 others(60): Show |
69 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.172-560T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31702567 | |||||||
| chr12:31702617 | G | A | 1 | a0001c0001t0003g0049 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.172-610C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31702617 | |||||||
| chr12:31702929 | G | T | 1 | a0001c0001t0003g0085 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.172-922C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31702929 | |||||||
| chr12:31703091 | A | C | 292 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(289): Show |
333 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.172-1084T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31703091 | |||||||
| chr12:31703111 | T | G | 4 | a0001c0001t0002g0179 a0001c0001t0002g0190 a0001c0001t0002g0192 others(1): Show |
4 | HG01346.hp1 HG01515.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-1104A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31703111 | |||||||
| chr12:31703189 | A | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0252 a0001c0001t0001g0254 others(1): Show |
8 | HG00597.hp2 NA18943.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.172-1182T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31703189 | |||||||
| chr12:31703383 | T | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-1376A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31703383 | |||||||
| chr12:31703398 | A | C | 68 | a0001c0001t0001g0115 a0001c0001t0002g0007 a0001c0001t0002g0013 others(65): Show |
74 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.172-1391T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31703398 | |||||||
| chr12:31703466 | G | A | 1 | a0001c0001t0001g0367 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.172-1459C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31703466 | |||||||
| chr12:31703589 | G | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-1582C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31703589 | |||||||
| chr12:31703747 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.172-1740T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31703747 | |||||||
| chr12:31703758 | T | G | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG02683.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.172-1751A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31703758 | |||||||
| chr12:31703931 | G | C | 9 | a0001c0001t0002g0016 a0001c0001t0002g0116 a0001c0001t0002g0117 others(6): Show |
10 | HG02451.hp2 HG02723.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-1924C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31703931 | |||||||
| chr12:31704152 | G | A | 1 | a0001c0001t0006g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.172-2145C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31704152 | |||||||
| chr12:31704331 | G | A | 6 | a0001c0001t0003g0002 a0001c0001t0003g0045 a0001c0001t0003g0091 others(3): Show |
9 | HG02523.hp2 NA18747.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-2324C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31704331 | |||||||
| chr12:31704336 | G | T | 1 | a0001c0001t0001g0210 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.172-2329C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31704336 | |||||||
| chr12:31704337 | T | C | 4 | a0001c0001t0002g0379 a0001c0001t0002g0380 a0001c0001t0002g0381 others(1): Show |
4 | HG02451.hp2 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-2330A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31704337 | |||||||
| chr12:31704351 | A | G | 68 | a0001c0001t0001g0115 a0001c0001t0002g0007 a0001c0001t0002g0013 others(65): Show |
74 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.172-2344T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31704351 | |||||||
| chr12:31704371 | GT | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-2365delA | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31704371 | |||||||
| chr12:31704373 | T | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-2366A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31704373 | |||||||
| chr12:31704496 | CT | C | 75 | a0001c0001t0001g0089 a0001c0001t0001g0115 a0001c0001t0001g0138 others(72): Show |
81 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.172-2490delA | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31704496 | |||||||
| chr12:31704537 | T | C | 1 | a0001c0001t0002g0171 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.172-2530A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31704537 | |||||||
| chr12:31704572 | T | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-2565A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31704572 | |||||||
| chr12:31704680 | T | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-2673A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31704680 | |||||||
| chr12:31704731 | A | T | 1 | a0001c0001t0001g0210 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.172-2724T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31704731 | |||||||
| chr12:31704751 | A | G | 3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0345 |
3 | HG00423.hp2 HG02040.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.172-2744T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31704751 | |||||||
| chr12:31704851 | G | C | 1 | a0001c0001t0002g0172 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.172-2844C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31704851 | |||||||
| chr12:31704932 | C | T | 3 | a0001c0001t0003g0091 a0001c0001t0003g0092 a0001c0001t0003g0093 |
3 | NA18974.hp2 NA19062.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.172-2925G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31704932 | |||||||
| chr12:31705052 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0144 a0001c0001t0001g0145 others(2): Show |
6 | HG02055.hp2 HG02647.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-3045G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31705052 | |||||||
| chr12:31705097 | G | A | 70 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(67): Show |
75 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.172-3090C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31705097 | |||||||
| chr12:31705155 | A | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-3148T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31705155 | |||||||
| chr12:31705293 | T | G | 28 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0106 others(25): Show |
34 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.172-3286A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31705293 | |||||||
| chr12:31705500 | A | G | 5 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(2): Show |
5 | HG01496.hp2 HG02300.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-3493T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31705500 | |||||||
| chr12:31705816 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.171+3477G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31705816 | |||||||
| chr12:31705912 | A | G | 35 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0106 others(32): Show |
41 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.171+3381T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31705912 | |||||||
| chr12:31706038 | C | T | 5 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(2): Show |
5 | HG02080.hp2 NA18952.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+3255G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706038 | |||||||
| chr12:31706039 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0181 a0001c0001t0001g0193 |
3 | HG02622.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.171+3254C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706039 | |||||||
| chr12:31706051 | G | A | 7 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0082 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+3242C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706051 | |||||||
| chr12:31706064 | G | C | 1 | a0001c0001t0001g0304 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.171+3229C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706064 | |||||||
| chr12:31706140 | G | A | 1 | a0001c0001t0003g0103 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.171+3153C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706140 | |||||||
| chr12:31706172 | T | C | 5 | a0001c0001t0002g0151 a0001c0001t0002g0166 a0001c0001t0002g0167 others(2): Show |
5 | HG00140.hp2 HG01169.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+3121A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706172 | |||||||
| chr12:31706311 | C | CA | 97 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(94): Show |
112 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.171+2981dupT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706311 | |||||||
| chr12:31706311 | C | CAA | 18 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0078 others(15): Show |
18 | HG00423.hp1 HG00558.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.171+2980_171+2981d others(4): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706311 | |||||||
| chr12:31706311 | CA | C | 72 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0024 others(69): Show |
78 | HG00544.hp1 HG00609.hp1 HG01069.hp2 others(75): Show |
intron_variant | MODIFIER | c.171+2981delT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706311 | |||||||
| chr12:31706311 | CAA | C | 12 | a0001c0001t0001g0141 a0001c0001t0001g0205 a0001c0001t0001g0206 others(9): Show |
12 | HG00323.hp2 HG01884.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.171+2980_171+2981d others(4): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706311 | |||||||
| chr12:31706311 | CAAAA | C | 44 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(41): Show |
46 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.171+2978_171+2981d others(6): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706311 | |||||||
| chr12:31706364 | T | C | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.171+2929A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706364 | |||||||
| chr12:31706413 | C | A | 2 | a0001c0001t0001g0323 a0001c0001t0001g0356 |
2 | HG03654.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.171+2880G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706413 | |||||||
| chr12:31706487 | C | A | 1 | a0001c0001t0001g0205 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.171+2806G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706487 | |||||||
| chr12:31706601 | A | T | 3 | a0001c0001t0002g0127 a0001c0001t0002g0134 a0001c0001t0002g0250 |
3 | NA18940.hp2 NA18974.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.171+2692T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706601 | |||||||
| chr12:31706626 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.171+2667G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706626 | |||||||
| chr12:31706639 | G | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+2654C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706639 | |||||||
| chr12:31706690 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.171+2603T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706690 | |||||||
| chr12:31706696 | C | T | 369 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(366): Show |
417 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(414): Show |
intron_variant | MODIFIER | c.171+2597G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706696 | |||||||
| chr12:31706713 | T | C | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG02723.hp2 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+2580A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706713 | |||||||
| chr12:31706788 | C | T | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+2505G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706788 | |||||||
| chr12:31706817 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+2476G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706817 | |||||||
| chr12:31706839 | T | C | 1 | a0001c0001t0003g0114 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.171+2454A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706839 | |||||||
| chr12:31706989 | TAAGAA | T | 68 | a0001c0001t0001g0115 a0001c0001t0002g0007 a0001c0001t0002g0013 others(65): Show |
74 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.171+2299_171+2303d others(7): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31706989 | |||||||
| chr12:31707005 | AGAT | A | 7 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0082 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+2285_171+2287d others(5): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31707005 | |||||||
| chr12:31707011 | A | C | 7 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0082 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+2282T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31707011 | |||||||
| chr12:31707013 | C | A | 7 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0082 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+2280G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31707013 | |||||||
| chr12:31707013 | C | CAA | 280 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
320 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.171+2279_171+2280i others(4): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31707013 | |||||||
| chr12:31707188 | A | AGAATAAA others(3): Show |
2 | a0001c0001t0001g0037 a0001c0001t0001g0348 |
2 | NA18939.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.171+2095_171+2104d others(12): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31707188 | |||||||
| chr12:31707202 | T | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+2091A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31707202 | |||||||
| chr12:31707208 | A | G | 24 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(21): Show |
24 | HG00438.hp2 HG02027.hp2 HG02129.hp1 others(21): Show |
intron_variant | MODIFIER | c.171+2085T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31707208 | |||||||
| chr12:31707256 | T | C | 53 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(50): Show |
55 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.171+2037A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31707256 | |||||||
| chr12:31707278 | G | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+2015C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31707278 | |||||||
| chr12:31707578 | T | C | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
4 | HG01496.hp2 HG02300.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.171+1715A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31707578 | |||||||
| chr12:31707614 | A | G | 1 | a0001c0001t0002g0184 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.171+1679T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31707614 | |||||||
| chr12:31707700 | T | C | 1 | a0001c0001t0001g0241 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.171+1593A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31707700 | |||||||
| chr12:31707725 | G | A | 4 | a0001c0001t0002g0379 a0001c0001t0002g0380 a0001c0001t0002g0381 others(1): Show |
4 | HG02451.hp2 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.171+1568C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31707725 | |||||||
| chr12:31707976 | T | A | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+1317A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31707976 | |||||||
| chr12:31707987 | G | A | 32 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0325 others(29): Show |
33 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.171+1306C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31707987 | |||||||
| chr12:31708093 | A | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+1200T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31708093 | |||||||
| chr12:31708196 | C | T | 1 | a0001c0001t0002g0179 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.171+1097G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31708196 | |||||||
| chr12:31708303 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0181 a0001c0001t0001g0193 |
3 | HG02622.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.171+990C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31708303 | |||||||
| chr12:31708360 | A | G | 369 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(366): Show |
417 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(414): Show |
intron_variant | MODIFIER | c.171+933T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31708360 | |||||||
| chr12:31708454 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0211 a0001c0001t0001g0214 others(1): Show |
6 | HG00423.hp1 HG00544.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.171+839C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31708454 | |||||||
| chr12:31708486 | G | A | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG02723.hp2 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+807C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31708486 | |||||||
| chr12:31708703 | G | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+590C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31708703 | |||||||
| chr12:31708766 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.171+527T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31708766 | |||||||
| chr12:31708826 | A | G | 39 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0036 others(36): Show |
42 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.171+467T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31708826 | |||||||
| chr12:31708949 | G | A | 3 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0358 |
3 | HG00438.hp1 HG02080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.171+344C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31708949 | |||||||
| chr12:31709064 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.171+229T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31709064 | |||||||
| chr12:31709098 | C | G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0181 a0001c0001t0001g0193 |
3 | HG02622.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.171+195G>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31709098 | |||||||
| chr12:31709173 | T | TA | 24 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0024 others(21): Show |
36 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.171+119dupT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 2/6 | chr12 | 31709173 | |||||||
| chr12:31709662 | A | G | 4 | a0001c0001t0002g0016 a0001c0001t0002g0116 a0001c0001t0002g0117 others(1): Show |
5 | HG02723.hp1 HG02818.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.39-237T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31709662 | |||||||
| chr12:31709729 | T | G | 1 | a0001c0001t0001g0241 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.39-304A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31709729 | |||||||
| chr12:31709794 | G | A | 4 | a0001c0001t0002g0016 a0001c0001t0002g0116 a0001c0001t0002g0117 others(1): Show |
5 | HG02723.hp1 HG02818.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.39-369C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31709794 | |||||||
| chr12:31709852 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.39-427T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31709852 | |||||||
| chr12:31709914 | C | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.39-489G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31709914 | |||||||
| chr12:31709988 | C | T | 1 | a0001c0001t0008g0353 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.39-563G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31709988 | |||||||
| chr12:31710006 | G | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0251 others(2): Show |
7 | HG00140.hp1 HG00642.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.39-581C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31710006 | |||||||
| chr12:31710066 | A | G | 5 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(2): Show |
5 | HG01496.hp2 HG02300.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.39-641T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31710066 | |||||||
| chr12:31710105 | T | C | 1 | a0001c0001t0003g0104 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.39-680A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31710105 | |||||||
| chr12:31710258 | A | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.39-833T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31710258 | |||||||
| chr12:31710551 | T | TAC | 109 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(106): Show |
129 | HG00280.hp2 HG00544.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.39-1128_39-1127dup others(2): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31710551 | |||||||
| chr12:31710551 | T | TACAC | 63 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(60): Show |
68 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.39-1130_39-1127dup others(4): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31710551 | |||||||
| chr12:31710551 | T | TACACAC | 16 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(13): Show |
16 | HG00609.hp1 HG01358.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.39-1132_39-1127dup others(6): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31710551 | |||||||
| chr12:31710551 | T | TACACACA others(1): Show |
5 | a0001c0001t0001g0141 a0001c0001t0001g0208 a0001c0001t0001g0284 others(2): Show |
5 | HG01943.hp1 HG03927.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.39-1134_39-1127dup others(8): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31710551 | |||||||
| chr12:31710551 | TAC | T | 101 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0031 others(98): Show |
110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.39-1128_39-1127del others(2): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31710551 | |||||||
| chr12:31710551 | TACAC | T | 14 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0350 others(11): Show |
15 | HG02155.hp1 HG02647.hp2 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.39-1130_39-1127del others(4): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31710551 | |||||||
| chr12:31710551 | TACACAC | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0278 a0001c0001t0001g0319 others(1): Show |
5 | HG00621.hp2 HG01891.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.39-1132_39-1127del others(6): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31710551 | |||||||
| chr12:31710551 | TACACACA others(1): Show |
T | 3 | a0001c0001t0001g0312 a0001c0001t0001g0316 a0001c0001t0001g0318 |
3 | HG00438.hp2 HG02129.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.39-1134_39-1127del others(8): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31710551 | |||||||
| chr12:31710551 | TACACACA others(5): Show |
T | 2 | a0001c0001t0001g0357 a0001c0001t0009g0360 |
2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.39-1138_39-1127del others(12): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31710551 | |||||||
| chr12:31710551 | TACACACA others(9): Show |
T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0024 others(20): Show |
34 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.39-1142_39-1127del others(16): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31710551 | |||||||
| chr12:31710658 | T | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.39-1233A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31710658 | |||||||
| chr12:31710934 | G | T | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.39-1509C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31710934 | |||||||
| chr12:31711021 | T | TG | 3 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0008g0353 |
3 | NA18978.hp2 NA18982.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.39-1597dupC | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31711021 | |||||||
| chr12:31711075 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0327 a0001c0001t0001g0328 |
4 | HG00323.hp1 NA18952.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.39-1650T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31711075 | |||||||
| chr12:31711219 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.39-1794G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31711219 | |||||||
| chr12:31711310 | T | G | 30 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0044 others(27): Show |
31 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.39-1885A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31711310 | |||||||
| chr12:31711365 | G | T | 1 | a0001c0001t0002g0183 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.39-1940C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31711365 | |||||||
| chr12:31711369 | T | A | 1 | a0001c0001t0001g0370 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.39-1944A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31711369 | |||||||
| chr12:31711771 | A | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.39-2346T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31711771 | |||||||
| chr12:31711804 | A | T | 1 | a0001c0001t0002g0158 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.39-2379T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31711804 | |||||||
| chr12:31711861 | C | T | 2 | a0001c0001t0001g0323 a0001c0001t0001g0356 |
2 | HG03654.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.39-2436G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31711861 | |||||||
| chr12:31712148 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.39-2723G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31712148 | |||||||
| chr12:31712256 | AT | A | 7 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0082 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.39-2832delA | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31712256 | |||||||
| chr12:31712274 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0024 others(21): Show |
36 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.39-2849C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31712274 | |||||||
| chr12:31712314 | G | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.39-2889C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31712314 | |||||||
| chr12:31712316 | C | T | 4 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0001c0001t0004g0055 others(1): Show |
4 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.39-2891G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31712316 | |||||||
| chr12:31712335 | C | T | 4 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0003g0084 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.39-2910G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31712335 | |||||||
| chr12:31712404 | C | T | 144 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(141): Show |
161 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.39-2979G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31712404 | |||||||
| chr12:31712570 | A | G | 1 | a0001c0001t0001g0038 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.39-3145T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31712570 | |||||||
| chr12:31712577 | T | G | 1 | a0001c0001t0001g0249 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.39-3152A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31712577 | |||||||
| chr12:31712600 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(102): Show |
126 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.39-3175G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31712600 | |||||||
| chr12:31712730 | A | T | 1 | a0001c0001t0001g0064 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.39-3305T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31712730 | |||||||
| chr12:31712899 | ACGCCTCG others(3): Show |
A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.39-3484_39-3475del others(10): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31712899 | |||||||
| chr12:31712911 | C | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.39-3486G>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31712911 | |||||||
| chr12:31712942 | C | T | 53 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(50): Show |
55 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.39-3517G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31712942 | |||||||
| chr12:31712978 | G | T | 1 | a0001c0001t0002g0157 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.39-3553C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31712978 | |||||||
| chr12:31713188 | G | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0011 others(59): Show |
80 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.39-3763C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31713188 | |||||||
| chr12:31713203 | TTCTC | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0251 others(2): Show |
7 | HG00140.hp1 HG00642.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.39-3782_39-3779del others(4): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31713203 | |||||||
| chr12:31713415 | C | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0181 a0001c0001t0001g0193 |
3 | HG02622.hp1 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.39-3990G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31713415 | |||||||
| chr12:31713423 | T | C | 45 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0036 others(42): Show |
48 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.39-3998A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31713423 | |||||||
| chr12:31713473 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(208): Show |
246 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.39-4048G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31713473 | |||||||
| chr12:31713667 | C | T | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.39-4242G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31713667 | |||||||
| chr12:31713865 | A | AT | 53 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(50): Show |
55 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.39-4441dupA | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31713865 | |||||||
| chr12:31713866 | T | A | 1 | a0001c0001t0001g0081 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.39-4441A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31713866 | |||||||
| chr12:31713899 | T | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0024 others(20): Show |
34 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.39-4474A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31713899 | |||||||
| chr12:31713899 | T | G | 190 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
214 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.39-4474A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31713899 | |||||||
| chr12:31713905 | G | A | 1 | a0001c0001t0004g0086 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.39-4480C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31713905 | |||||||
| chr12:31713944 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0010g0213 |
2 | HG02083.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.39-4519T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31713944 | |||||||
| chr12:31714047 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.39-4622C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31714047 | |||||||
| chr12:31714155 | A | C | 39 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0036 others(36): Show |
42 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.39-4730T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31714155 | |||||||
| chr12:31714156 | A | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG02129.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.39-4731T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31714156 | |||||||
| chr12:31714252 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.39-4827A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31714252 | |||||||
| chr12:31714394 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.39-4969T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31714394 | |||||||
| chr12:31714478 | C | A | 6 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
6 | HG02027.hp2 NA18962.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.39-5053G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31714478 | |||||||
| chr12:31714573 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(102): Show |
126 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.39-5148G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31714573 | |||||||
| chr12:31714663 | A | C | 7 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0082 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.39-5238T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31714663 | |||||||
| chr12:31714922 | A | C | 77 | a0001c0001t0001g0115 a0001c0001t0002g0007 a0001c0001t0002g0013 others(74): Show |
84 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.39-5497T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31714922 | |||||||
| chr12:31715092 | T | C | 49 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(46): Show |
51 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.39-5667A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31715092 | |||||||
| chr12:31715201 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.39-5776C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31715201 | |||||||
| chr12:31715227 | C | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0024 others(21): Show |
36 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.39-5802G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31715227 | |||||||
| chr12:31715265 | A | G | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
4 | HG02683.hp1 HG03710.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.39-5840T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31715265 | |||||||
| chr12:31715286 | T | C | 1 | a0001c0001t0001g0303 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.39-5861A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31715286 | |||||||
| chr12:31715452 | C | T | 64 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(61): Show |
69 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.39-6027G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31715452 | |||||||
| chr12:31715492 | T | C | 1 | a0001c0001t0001g0370 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.39-6067A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31715492 | |||||||
| chr12:31715556 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.39-6131G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31715556 | |||||||
| chr12:31715572 | G | A | 1 | a0001c0001t0001g0367 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.39-6147C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31715572 | |||||||
| chr12:31715580 | G | A | 377 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(374): Show |
425 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(422): Show |
intron_variant | MODIFIER | c.39-6155C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31715580 | |||||||
| chr12:31715593 | A | C | 1 | a0001c0001t0002g0182 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.39-6168T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31715593 | |||||||
| chr12:31715900 | T | G | 368 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(365): Show |
416 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(413): Show |
intron_variant | MODIFIER | c.39-6475A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31715900 | |||||||
| chr12:31716034 | A | C | 67 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(64): Show |
72 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.39-6609T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31716034 | |||||||
| chr12:31716160 | C | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG01192.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.39-6735G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31716160 | |||||||
| chr12:31716345 | G | A | 1 | a0001c0001t0001g0259 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.39-6920C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31716345 | |||||||
| chr12:31716397 | T | C | 2 | a0001c0001t0005g0371 a0001c0001t0005g0372 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.39-6972A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31716397 | |||||||
| chr12:31716464 | A | G | 4 | a0001c0001t0002g0379 a0001c0001t0002g0380 a0001c0001t0002g0381 others(1): Show |
4 | HG02451.hp2 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.39-7039T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31716464 | |||||||
| chr12:31716685 | T | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.39-7260A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31716685 | |||||||
| chr12:31716690 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.39-7265A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31716690 | |||||||
| chr12:31716736 | G | A | 4 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0001c0001t0004g0055 others(1): Show |
4 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.39-7311C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31716736 | |||||||
| chr12:31716758 | G | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.39-7333C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31716758 | |||||||
| chr12:31717004 | G | C | 7 | a0001c0001t0001g0350 a0001c0001t0001g0351 a0001c0001t0001g0352 others(4): Show |
7 | HG02155.hp1 NA18978.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.39-7579C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31717004 | |||||||
| chr12:31717115 | C | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.39-7690G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31717115 | |||||||
| chr12:31717207 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.39-7782G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31717207 | |||||||
| chr12:31717270 | C | T | 67 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(64): Show |
72 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.39-7845G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31717270 | |||||||
| chr12:31717592 | T | C | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
336 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.39-8167A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31717592 | |||||||
| chr12:31717593 | G | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.39-8168C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31717593 | |||||||
| chr12:31717879 | A | C | 1 | a0001c0001t0001g0261 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.39-8454T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31717879 | |||||||
| chr12:31717879 | A | G | 63 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(60): Show |
68 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.39-8454T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31717879 | |||||||
| chr12:31718036 | A | G | 1 | a0001c0001t0001g0311 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.39-8611T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31718036 | |||||||
| chr12:31718407 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.39-8982T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31718407 | |||||||
| chr12:31718420 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.39-8995G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31718420 | |||||||
| chr12:31718490 | A | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.39-9065T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31718490 | |||||||
| chr12:31718647 | T | G | 1 | a0001c0001t0002g0020 | 2 | HG00408.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.39-9222A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31718647 | |||||||
| chr12:31718720 | T | C | 1 | a0001c0001t0001g0014 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.39-9295A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31718720 | |||||||
| chr12:31718737 | C | T | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.39-9312G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31718737 | |||||||
| chr12:31718739 | T | G | 69 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(66): Show |
74 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.39-9314A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31718739 | |||||||
| chr12:31718937 | C | T | 5 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0001c0001t0004g0055 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.39-9512G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31718937 | |||||||
| chr12:31718960 | A | T | 3 | a0001c0001t0002g0018 a0001c0001t0002g0152 a0001c0001t0002g0248 |
4 | HG00558.hp2 NA18939.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.39-9535T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31718960 | |||||||
| chr12:31719065 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.39-9640C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31719065 | |||||||
| chr12:31719161 | C | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0147 a0001c0001t0001g0148 |
4 | HG02055.hp2 HG02965.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.39-9736G>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31719161 | |||||||
| chr12:31719169 | G | A | 1 | a0001c0002t0001g0273 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.39-9744C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31719169 | |||||||
| chr12:31719217 | C | T | 4 | a0001c0002t0001g0273 a0001c0002t0001g0321 a0001c0002t0007g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.38+9754G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31719217 | |||||||
| chr12:31719299 | A | G | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.38+9672T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31719299 | |||||||
| chr12:31719395 | A | G | 1 | a0001c0001t0001g0249 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.38+9576T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31719395 | |||||||
| chr12:31719497 | A | G | 1 | a0001c0001t0002g0180 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.38+9474T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31719497 | |||||||
| chr12:31719544 | A | G | 1 | a0001c0002t0007g0274 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.38+9427T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31719544 | |||||||
| chr12:31719750 | G | C | 1 | a0001c0001t0001g0046 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.38+9221C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31719750 | |||||||
| chr12:31719939 | G | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+9032C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31719939 | |||||||
| chr12:31720088 | T | C | 7 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0082 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.38+8883A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31720088 | |||||||
| chr12:31720303 | A | G | 5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(2): Show |
5 | HG01884.hp1 HG02258.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.38+8668T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31720303 | |||||||
| chr12:31720313 | T | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+8658A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31720313 | |||||||
| chr12:31720396 | C | T | 2 | a0001c0001t0002g0200 a0001c0001t0002g0201 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.38+8575G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31720396 | |||||||
| chr12:31720444 | G | A | 7 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0082 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.38+8527C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31720444 | |||||||
| chr12:31720445 | C | T | 7 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0082 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.38+8526G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31720445 | |||||||
| chr12:31720481 | A | G | 5 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(2): Show |
5 | HG01496.hp2 HG02300.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.38+8490T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31720481 | |||||||
| chr12:31720494 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.38+8477G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31720494 | |||||||
| chr12:31720540 | C | CA | 69 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(66): Show |
74 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.38+8430dupT | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31720540 | |||||||
| chr12:31720713 | G | T | 1 | a0001c0001t0001g0060 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.38+8258C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31720713 | |||||||
| chr12:31720894 | A | G | 1 | a0001c0001t0005g0374 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.38+8077T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31720894 | |||||||
| chr12:31720914 | C | T | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+8057G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31720914 | |||||||
| chr12:31721003 | C | T | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+7968G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31721003 | |||||||
| chr12:31721069 | A | G | 1 | a0001c0001t0001g0326 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.38+7902T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31721069 | |||||||
| chr12:31721147 | C | T | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+7824G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31721147 | |||||||
| chr12:31721204 | A | G | 4 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.38+7767T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31721204 | |||||||
| chr12:31721536 | A | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+7435T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31721536 | |||||||
| chr12:31721554 | C | G | 1 | a0001c0001t0001g0285 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.38+7417G>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31721554 | |||||||
| chr12:31721560 | A | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+7411T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31721560 | |||||||
| chr12:31721665 | T | A | 1 | a0001c0001t0001g0032 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.38+7306A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31721665 | |||||||
| chr12:31721889 | A | C | 2 | a0001c0001t0005g0371 a0001c0001t0005g0372 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.38+7082T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31721889 | |||||||
| chr12:31722003 | C | T | 4 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0001c0001t0004g0055 others(1): Show |
4 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.38+6968G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31722003 | |||||||
| chr12:31722073 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.38+6898C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31722073 | |||||||
| chr12:31722130 | G | GAC | 33 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(30): Show |
36 | HG00438.hp2 HG01167.hp1 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.38+6839_38+6840dup others(2): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31722130 | |||||||
| chr12:31722130 | G | GACAC | 12 | a0001c0001t0001g0135 a0001c0001t0001g0144 a0001c0001t0001g0193 others(9): Show |
12 | HG01099.hp2 HG02717.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.38+6837_38+6840dup others(4): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31722130 | |||||||
| chr12:31722130 | G | GACACAC | 6 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0145 others(3): Show |
6 | HG02647.hp2 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.38+6835_38+6840dup others(6): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31722130 | |||||||
| chr12:31722130 | G | GACACACA others(5): Show |
3 | a0001c0001t0002g0379 a0001c0001t0002g0380 a0001c0001t0011g0382 |
3 | HG02451.hp2 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.38+6829_38+6840dup others(12): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31722130 | |||||||
| chr12:31722130 | GAC | G | 27 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(24): Show |
27 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.38+6839_38+6840del others(2): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31722130 | |||||||
| chr12:31722130 | GACAC | G | 44 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0113 others(41): Show |
49 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.38+6837_38+6840del others(4): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31722130 | |||||||
| chr12:31722130 | GACACAC | G | 82 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(79): Show |
92 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.38+6835_38+6840del others(6): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31722130 | |||||||
| chr12:31722130 | GACACACA others(1): Show |
G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(66): Show |
89 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.38+6833_38+6840del others(8): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31722130 | |||||||
| chr12:31722130 | GACACACA others(3): Show |
G | 44 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(41): Show |
50 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.38+6831_38+6840del others(10): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31722130 | |||||||
| chr12:31722130 | GACACACA others(5): Show |
G | 6 | a0001c0001t0001g0052 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG00733.hp2 HG02258.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.38+6829_38+6840del others(12): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31722130 | |||||||
| chr12:31722130 | GACACACA others(9): Show |
G | 1 | a0001c0001t0001g0051 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.38+6825_38+6840del others(16): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31722130 | |||||||
| chr12:31722256 | G | T | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+6715C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31722256 | |||||||
| chr12:31722281 | T | G | 1 | a0001c0001t0002g0199 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.38+6690A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31722281 | |||||||
| chr12:31722436 | C | T | 5 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(2): Show |
5 | HG01496.hp2 HG02300.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.38+6535G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31722436 | |||||||
| chr12:31722600 | G | A | 1 | a0001c0001t0003g0114 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.38+6371C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31722600 | |||||||
| chr12:31722970 | A | C | 1 | a0001c0001t0001g0210 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.38+6001T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31722970 | |||||||
| chr12:31723109 | G | T | 1 | a0001c0001t0001g0047 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.38+5862C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31723109 | |||||||
| chr12:31723117 | C | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.38+5854G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31723117 | |||||||
| chr12:31723192 | A | T | 1 | a0001c0001t0001g0050 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.38+5779T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31723192 | |||||||
| chr12:31723225 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0146 |
2 | HG01123.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.38+5746G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31723225 | |||||||
| chr12:31723293 | G | C | 2 | a0001c0001t0002g0381 a0001c0001t0011g0382 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.38+5678C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31723293 | |||||||
| chr12:31723384 | C | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(48): Show |
63 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.38+5587G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31723384 | |||||||
| chr12:31723478 | G | T | 289 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
329 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.38+5493C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31723478 | |||||||
| chr12:31723551 | C | G | 1 | a0001c0004t0002g0383 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.38+5420G>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31723551 | |||||||
| chr12:31723732 | A | G | 64 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(61): Show |
69 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.38+5239T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31723732 | |||||||
| chr12:31723741 | C | G | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG02723.hp2 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.38+5230G>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31723741 | |||||||
| chr12:31723820 | C | T | 1 | a0001c0001t0003g0049 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.38+5151G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31723820 | |||||||
| chr12:31724015 | G | C | 5 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.38+4956C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31724015 | |||||||
| chr12:31724173 | T | C | 60 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(57): Show |
65 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.38+4798A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31724173 | |||||||
| chr12:31724244 | G | A | 64 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(61): Show |
69 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.38+4727C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31724244 | |||||||
| chr12:31724253 | G | A | 1 | a0001c0001t0002g0209 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.38+4718C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31724253 | |||||||
| chr12:31724355 | G | A | 50 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
62 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.38+4616C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31724355 | |||||||
| chr12:31724369 | T | C | 1 | a0001c0001t0001g0318 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.38+4602A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31724369 | |||||||
| chr12:31724460 | TTCA | T | 3 | a0001c0001t0002g0127 a0001c0001t0002g0134 a0001c0001t0002g0250 |
3 | NA18940.hp2 NA18974.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.38+4508_38+4510del others(3): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31724460 | |||||||
| chr12:31724480 | G | C | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.38+4491C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31724480 | |||||||
| chr12:31724698 | C | G | 53 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(50): Show |
55 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.38+4273G>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31724698 | |||||||
| chr12:31724849 | A | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG02129.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.38+4122T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31724849 | |||||||
| chr12:31724864 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.38+4107A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31724864 | |||||||
| chr12:31725217 | T | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
5 | NA18969.hp1 NA18984.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+3754A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31725217 | |||||||
| chr12:31725264 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.38+3707G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31725264 | |||||||
| chr12:31725294 | G | T | 1 | a0001c0001t0001g0249 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.38+3677C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31725294 | |||||||
| chr12:31725308 | G | C | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.38+3663C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31725308 | |||||||
| chr12:31725341 | C | T | 2 | a0001c0002t0001g0273 a0001c0002t0001g0321 |
2 | HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.38+3630G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31725341 | |||||||
| chr12:31725398 | A | G | 1 | a0001c0001t0001g0249 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.38+3573T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31725398 | |||||||
| chr12:31725408 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.38+3563G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31725408 | |||||||
| chr12:31725409 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.38+3562C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31725409 | |||||||
| chr12:31725430 | A | T | 377 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(374): Show |
425 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(422): Show |
intron_variant | MODIFIER | c.38+3541T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31725430 | |||||||
| chr12:31725536 | C | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.38+3435G>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31725536 | |||||||
| chr12:31725551 | G | A | 1 | a0001c0001t0002g0248 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.38+3420C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31725551 | |||||||
| chr12:31725553 | G | A | 1 | a0001c0001t0003g0119 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.38+3418C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31725553 | |||||||
| chr12:31725851 | A | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0270 a0001c0001t0001g0271 others(2): Show |
7 | HG00544.hp1 NA18955.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.38+3120T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31725851 | |||||||
| chr12:31726084 | C | T | 1 | a0001c0001t0001g0320 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.38+2887G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726084 | |||||||
| chr12:31726090 | A | G | 4 | a0001c0001t0002g0379 a0001c0001t0002g0380 a0001c0001t0002g0381 others(1): Show |
4 | HG02451.hp2 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.38+2881T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726090 | |||||||
| chr12:31726161 | C | CT | 274 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
305 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.38+2809dupA | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726161 | |||||||
| chr12:31726161 | C | CTT | 6 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0323 others(3): Show |
6 | HG01261.hp1 HG02738.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.38+2808_38+2809dup others(2): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726161 | |||||||
| chr12:31726175 | T | G | 1 | a0001c0001t0001g0029 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.38+2796A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726175 | |||||||
| chr12:31726175 | T | TG | 65 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0038 others(62): Show |
70 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.38+2795dupC | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726175 | |||||||
| chr12:31726176 | G | T | 2 | a0001c0001t0005g0371 a0001c0001t0005g0372 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.38+2795C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726176 | |||||||
| chr12:31726187 | G | A | 1 | a0001c0001t0001g0319 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.38+2784C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726187 | |||||||
| chr12:31726218 | A | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+2753T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726218 | |||||||
| chr12:31726266 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.38+2705T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726266 | |||||||
| chr12:31726323 | G | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+2648C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726323 | |||||||
| chr12:31726395 | A | C | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.38+2576T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726395 | |||||||
| chr12:31726441 | G | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+2530C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726441 | |||||||
| chr12:31726668 | A | G | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2303T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726668 | |||||||
| chr12:31726669 | ATTACTAG others(7): Show |
A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2288_38+2301del others(14): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726669 | |||||||
| chr12:31726678 | C | T | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+2293G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726678 | |||||||
| chr12:31726685 | A | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2286T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726685 | |||||||
| chr12:31726690 | T | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2281A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726690 | |||||||
| chr12:31726691 | C | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2280G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726691 | |||||||
| chr12:31726697 | T | G | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2274A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726697 | |||||||
| chr12:31726701 | T | C | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2270A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726701 | |||||||
| chr12:31726704 | A | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2267T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726704 | |||||||
| chr12:31726707 | C | G | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2264G>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726707 | |||||||
| chr12:31726709 | A | C | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2262T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726709 | |||||||
| chr12:31726710 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2261C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726710 | |||||||
| chr12:31726711 | A | C | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2260T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726711 | |||||||
| chr12:31726713 | A | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2258T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726713 | |||||||
| chr12:31726716 | G | C | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2255C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726716 | |||||||
| chr12:31726717 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2254G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726717 | |||||||
| chr12:31726722 | T | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2249A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726722 | |||||||
| chr12:31726724 | A | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2247T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726724 | |||||||
| chr12:31726728 | A | G | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2243T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726728 | |||||||
| chr12:31726740 | A | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2231T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726740 | |||||||
| chr12:31726744 | T | G | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2227A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726744 | |||||||
| chr12:31726747 | A | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2224T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726747 | |||||||
| chr12:31726756 | C | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2215G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726756 | |||||||
| chr12:31726757 | A | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2214T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726757 | |||||||
| chr12:31726763 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2208C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726763 | |||||||
| chr12:31726764 | T | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2207A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726764 | |||||||
| chr12:31726768 | A | G | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2203T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726768 | |||||||
| chr12:31726769 | A | G | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2202T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726769 | |||||||
| chr12:31726770 | A | G | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2201T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726770 | |||||||
| chr12:31726771 | T | C | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2200A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726771 | |||||||
| chr12:31726773 | A | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2198T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726773 | |||||||
| chr12:31726781 | A | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2190T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726781 | |||||||
| chr12:31726783 | G | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2188C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726783 | |||||||
| chr12:31726784 | G | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2187C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726784 | |||||||
| chr12:31726786 | A | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2185T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726786 | |||||||
| chr12:31726788 | A | G | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2183T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726788 | |||||||
| chr12:31726789 | T | C | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2182A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726789 | |||||||
| chr12:31726792 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2179C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726792 | |||||||
| chr12:31726793 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2178C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726793 | |||||||
| chr12:31726795 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2176G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726795 | |||||||
| chr12:31726797 | T | C | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2174A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726797 | |||||||
| chr12:31726805 | G | C | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2166C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726805 | |||||||
| chr12:31726806 | G | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2165C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726806 | |||||||
| chr12:31726827 | A | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2144T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726827 | |||||||
| chr12:31726831 | A | G | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2140T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726831 | |||||||
| chr12:31726832 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2139C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726832 | |||||||
| chr12:31726838 | G | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2133C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726838 | |||||||
| chr12:31726839 | T | G | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2132A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726839 | |||||||
| chr12:31726840 | A | G | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2131T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726840 | |||||||
| chr12:31726841 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2130C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726841 | |||||||
| chr12:31726848 | C | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2123G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726848 | |||||||
| chr12:31726851 | T | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2120A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726851 | |||||||
| chr12:31726863 | G | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2108C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726863 | |||||||
| chr12:31726866 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2105G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726866 | |||||||
| chr12:31726873 | A | C | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2098T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726873 | |||||||
| chr12:31726874 | T | G | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2097A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726874 | |||||||
| chr12:31726875 | T | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2096A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726875 | |||||||
| chr12:31726876 | T | G | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2095A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726876 | |||||||
| chr12:31726877 | T | G | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2094A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726877 | |||||||
| chr12:31726878 | T | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2093A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726878 | |||||||
| chr12:31726879 | C | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2092G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726879 | |||||||
| chr12:31726880 | T | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2091A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726880 | |||||||
| chr12:31726881 | T | G | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2090A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726881 | |||||||
| chr12:31726883 | A | G | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2088T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726883 | |||||||
| chr12:31726884 | C | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2087G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726884 | |||||||
| chr12:31726886 | T | G | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2085A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726886 | |||||||
| chr12:31726887 | T | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2084A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726887 | |||||||
| chr12:31726888 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2083C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726888 | |||||||
| chr12:31726893 | T | C | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2078A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726893 | |||||||
| chr12:31726894 | C | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2077G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726894 | |||||||
| chr12:31726895 | T | G | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2076A>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726895 | |||||||
| chr12:31726896 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2075C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726896 | |||||||
| chr12:31726897 | T | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2074A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726897 | |||||||
| chr12:31726900 | C | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+2071G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726900 | |||||||
| chr12:31726953 | T | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+2018A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726953 | |||||||
| chr12:31726968 | CATTTATT others(5): Show |
C | 87 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(84): Show |
97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.38+1991_38+2002del others(12): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31726968 | |||||||
| chr12:31727003 | C | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.38+1968G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31727003 | |||||||
| chr12:31727006 | G | T | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.38+1965C>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31727006 | |||||||
| chr12:31727223 | A | G | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.38+1748T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31727223 | |||||||
| chr12:31727266 | G | A | 1 | a0001c0002t0001g0321 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.38+1705C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31727266 | |||||||
| chr12:31727266 | G | C | 1 | a0001c0001t0001g0320 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.38+1705C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31727266 | |||||||
| chr12:31727579 | A | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+1392T>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31727579 | |||||||
| chr12:31727641 | G | C | 1 | a0001c0001t0001g0322 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.38+1330C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31727641 | |||||||
| chr12:31727773 | GCA | G | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+1196_38+1197del others(2): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31727773 | |||||||
| chr12:31727777 | CCT | C | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+1192_38+1193del others(2): Show |
AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31727777 | |||||||
| chr12:31727780 | A | T | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+1191T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31727780 | |||||||
| chr12:31727783 | C | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+1188G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31727783 | |||||||
| chr12:31727816 | T | A | 49 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(46): Show |
51 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.38+1155A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31727816 | |||||||
| chr12:31727924 | G | A | 1 | a0001c0001t0001g0369 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.38+1047C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31727924 | |||||||
| chr12:31728089 | G | C | 87 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(84): Show |
97 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.38+882C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31728089 | |||||||
| chr12:31728207 | A | G | 93 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(90): Show |
103 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.38+764T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31728207 | |||||||
| chr12:31728257 | T | A | 1 | a0001c0001t0001g0370 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.38+714A>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31728257 | |||||||
| chr12:31728276 | T | C | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+695A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31728276 | |||||||
| chr12:31728278 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+693G>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31728278 | |||||||
| chr12:31728285 | A | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+686T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31728285 | |||||||
| chr12:31728295 | G | C | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+676C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31728295 | |||||||
| chr12:31728301 | A | T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.38+670T>A | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31728301 | |||||||
| chr12:31728326 | G | A | 5 | a0001c0001t0005g0371 a0001c0001t0005g0372 a0001c0001t0005g0373 others(2): Show |
5 | HG02809.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.38+645C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31728326 | |||||||
| chr12:31728490 | T | C | 1 | a0001c0001t0001g0032 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.38+481A>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31728490 | |||||||
| chr12:31728501 | G | A | 1 | a0001c0001t0001g0376 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.38+470C>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31728501 | |||||||
| chr12:31728517 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.38+454T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31728517 | |||||||
| chr12:31728562 | C | A | 1 | a0001c0001t0001g0377 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.38+409G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31728562 | |||||||
| chr12:31728563 | C | A | 1 | a0001c0001t0001g0377 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.38+408G>T | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31728563 | |||||||
| chr12:31728576 | A | G | 3 | a0001c0001t0002g0013 a0001c0001t0002g0034 a0001c0001t0002g0035 |
4 | HG02109.hp1 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.38+395T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31728576 | |||||||
| chr12:31728775 | A | G | 1 | a0001c0001t0002g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.38+196T>C | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31728775 | |||||||
| chr12:31728869 | G | C | 5 | a0001c0001t0002g0379 a0001c0001t0002g0380 a0001c0001t0002g0381 others(2): Show |
5 | HG02451.hp2 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.38+102C>G | AMN1 | ENSG00000151743.11 | transcript | ENST00000281471.11 | protein_coding | 1/6 | chr12 | 31728869 |